HYSTEROSCOPE— 510(k) K934286

Substantially Equivalent

Bei Medical Systems Co., Inc.

FDA 510(k) clearance K934286 for HYSTEROSCOPE, Substantially Equivalent on 1994-07-19. Applicant: Bei Medical Systems Co., Inc..

Clearance details

Applicant: Bei Medical Systems Co., Inc.
Product code: Code HIH
Advisory panel: Obstetrics/Gynecology
Date received: 1993-09-02
Decision date: 1994-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hackensack, NJ, US

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Adverse events under product code HIH

product code HIH

Death: 18
Injury: 973
Malfunction: 5,071
Other: 1
Total: 6,063

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.