MICRO-AIRE POWERED MICRO-SURGERY INSTRUMENTS— 510(k) K900033

Substantially Equivalent

Micro-Aire Surgical Instruments, Inc.

FDA 510(k) clearance K900033 for MICRO-AIRE POWERED MICRO-SURGERY INSTRUMENTS, Substantially Equivalent on 1990-02-13. Applicant: Micro-Aire Surgical Instruments, Inc..

Clearance details

Applicant: Micro-Aire Surgical Instruments, Inc.
Product code: Code GEY
Advisory panel: General, Plastic Surgery
Date received: 1990-01-02
Decision date: 1990-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Valencia, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code GEY

product code GEY

Malfunction: 7,488
Total: 7,488

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.