ASSI
ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION · Model ASSI.SDCT18R8T · UDI-DI 00841645136453
10
510(k) clearances
67
Adverse events (1 deaths)
1
Recalls
137
Facilities
Description
Diss. Sciss. (Titanium) 18cm Lg. Rnd. Hdl. 8mm Dia., Cvd. Serr. Blds. 12mm Lg.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-01-22 | Medtronic Xomed, Inc. | A labeling discrepancy was internally identified for the surface electrode component of REF 8263210 AccuGuide EMG Injection Needle, 30G X 25MM. The outside box label correctly ind |
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.
