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., part of PhilipsLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Advanced Technology Laboratories with 61 510(k) clearances. The most recent is a 510(k) clearance dated Jul 2, 2002: Q LAB SOFTWARE.
| Jul 2, 2002 | Q LAB SOFTWAREK021966 · LLZ | 510(k) clearances |
| May 4, 2001 | HDI 5000 ULTRASOUND SYSTEM WITH ASSISTED BORDER DETECTION (ABD), XRES IMAGING, AND PANORAMIC MEASUREMENT CAPABILITYK011224 · IYN | 510(k) clearances |
| Sep 28, 2000 | MEDLINK DIAGNOSTIC OFFLINE WORKSTATIONK002144 · LLZ | 510(k) clearances |
| Aug 23, 1999 | ULTRAMARK 400C/SONOACE 6000 ULTRASOUND SYSTEMK992470 · IYO | 510(k) clearances |
| Jun 18, 1999 | HDI 5000 DIAGNOSTIC ULTRASOUND SYSTEMK991671 · IYO | 510(k) clearances |
| Mar 26, 1997 | LEVEL 10 HDIK961459 · IYO | 510(k) clearances |
| Oct 11, 1994 | PEGASUSK935009 · IYN | 510(k) clearances |
| Jul 29, 1994 | NOVA MICROSONICS ACCESS IMAGE MANAGEMENT NETWORK/ACCESS ACQUISITION MODULEK940423 · LMD | 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
