Home › AMBLER SURGICAL CORP. › Ambler Surgical
Ambler Surgical
AMBLER SURGICAL CORP. · Model Fiberoptic light cable · UDI-DI 00190660100643
EQH
Prescription
10
510(k) clearances
36
Adverse events
1
Recalls
99
Facilities
Description
Fiberoptic light cable, 7 1/2' length x 3.5mm bundle diameter, gray sheathing, Karl Storz scope / Karl Storz light source (threaded) connectors
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-07 | Boston Scientific Corporation | Light Degradation in transmission-A film may deposit on the front face and limit transmission of light |
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.