Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Michigan Instruments, Inc. with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Feb 13, 2018: Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: ….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 13, 2018 | Thumper Cardiopulmonary Resuscitator, Model 1007CCV, Catalog No. 15370 Product Usage: The device is used to perform Cardiopulmonary ResuscClass III · A performance issue with the chest depth needle valve (CDNV) may arise where turning the knob will not deliver any compr | Device recalls |
| Feb 14, 2008 | THUMPER, MODEL: 1008K073079 · DRM | 510(k) clearances |
| Oct 2, 1997 | THUMPERK972525 · DRM | 510(k) clearances |
| Sep 5, 1996 | THUMPER CARDIOPULMONARY RESUSCITATORK962237 · DRM | 510(k) clearances |
| Oct 30, 1989 | LARYNGOSTAT LARYNGOSCOPE HANDLEK895954 · CCW | 510(k) clearances |
| May 15, 1985 | THUMPER CARDIOPULMONARY RESUSCITATOR 1005K851139 · DRM | 510(k) clearances |
| Dec 27, 1983 | CARDIOPULMONARY RESUSCITATORK833879 · DRM | 510(k) clearances |
| Jul 16, 1981 | CARDIOPULMUNARY RESUSCITATORK811909 · DRM | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
