Home › MIDMARK CORPORATION › Midmark
Midmark
MIDMARK CORPORATION · Model 604 Manual Examination Table · UDI-DI 00841709106071
4
510(k) clearances
652
Adverse events (1 deaths)
1
Recalls
68
Facilities
Description
The Midmark 604 Manual Examination Table is intended to be used as a table to provide positioning and support of patients during examination procedures conducted by qualified medical professionals in an office environment.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-05-12 | Stryker Medical Division of Stryker Corporation | Medical devices intended for use in a healthcare facility were distributed to residential customers and may be in use in a home environment. The product s labeling accurately iden |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.