Home › ELMED INCORPORATED › ELMED INCORPORATED
ELMED INCORPORATED
ELMED INCORPORATED · Model 222 167-07 · UDI-DI 00198506089459
BRX
Prescription
1
510(k) clearances
2
Adverse events
1
Recalls
2
Facilities
Description
KNOB FOR BACKREST ADJUSTMENT ON SURGEONS STOOL 222 167
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2019-07-10 | Gk Photonics Inc | The User Remote Interlock Dongle provided with the E-Stop Remote is not sufficient to fully comply with the FDA's Manual Reset Mechanism requirement for laser projectors and could |
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.
