AESCULAP LAPAROSCOPIC ANCILLARY DEVICES— 510(k) K943603

Substantially Equivalent

Aesculap, Inc.

FDA 510(k) clearance K943603 for AESCULAP LAPAROSCOPIC ANCILLARY DEVICES, Substantially Equivalent on 1995-03-29. Applicant: Aesculap, Inc..

Clearance details

Applicant: Aesculap, Inc.
Product code: Code HET
Advisory panel: Obstetrics/Gynecology
Date received: 1994-07-25
Decision date: 1995-03-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code HET

product code HET

Malfunction: 10,504
Total: 10,504

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.