FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE— 510(k) K933770

Substantially Equivalent

Mahe-Medizintechnik

FDA 510(k) clearance K933770 for FORCEPS, ENT INSTR, ENT MANUAL SURG RETRACT/ALL TYPE, Substantially Equivalent on 1994-03-23. Applicant: Mahe-Medizintechnik.

Clearance details

Applicant: Mahe-Medizintechnik
Product code: Code LRC
Advisory panel: Ear, Nose, Throat
Date received: 1993-07-29
Decision date: 1994-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Nashville, TN, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code LRC

product code LRC

Death: 5
Total: 5

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.