Medical device makerLabelled 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 13, 2026, FDA's public records list Vidco with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Nov 8, 2015: Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3,….
| Date | Record | Source |
|---|---|---|
| Nov 8, 2015 | Remote Patient Monitoring System, MDP 2000 Series, Part Numbers: MDP2040-0100, PGM340R3, or PGM340R4. The MDP2000 is intended for use in Class II · Testing at customer site showed unit Remote Patient Monitoring System MDP2040-0100 in a continuous trap condition, not a | Device recalls |
| Oct 22, 1997 | MDP2000 MEDICAL DATA PROCESSORK972880 · MSX | 510(k) clearances |
| Aug 18, 1994 | 580CDR DISPLAY DRIVERK934093 · DXJ | 510(k) clearances |
| Jun 20, 1994 | 620CSR DISPLAY DRIVERK932894 · DXJ | 510(k) clearances |
| May 4, 1994 | 520 DISPLAY DRIVER- STATUS IK926298 · DRT | 510(k) clearances |
| Dec 16, 1993 | 516YT DISPLAY DRIVERK926219 · DXJ | 510(k) clearances |
| Nov 8, 1993 | 580CD DISPLAY DRIVERK926162 · DXJ | 510(k) clearances |
| Mar 2, 1989 | SMDS460 SURGICAL MONITOR DISPLAY SYSTEMK890353 · DXJ | 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
