AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS— 510(k) K924725

Substantially Equivalent

American Biomaterials Corp.

FDA 510(k) clearance K924725 for AMERICAN BIOMED, INC. MICROSURGICAL INSTRUMENTS, Substantially Equivalent on 1993-02-05. Applicant: American Biomaterials Corp..

Clearance details

Applicant: American Biomaterials Corp.
Product code: Code MDM
Advisory panel: General, Plastic Surgery
Date received: 1992-09-21
Decision date: 1993-02-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: The Woodlands, TX, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code MDM

product code MDM

Injury: 247
Malfunction: 1,516
Total: 1,763

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.