A4907 LENS CLEANING SHEATH— 510(k) K961860

Name: FDA 510(k) clearance K961860
Creator: U.S. Food and Drug Administration
Published: 1996-08-29

Substantially Equivalent

Olympus America, Inc.

FDA 510(k) clearance K961860 for A4907 LENS CLEANING SHEATH, Substantially Equivalent on 1996-08-29. Applicant: Olympus America, Inc.. Device class: 2.

Clearance details

Applicant: Olympus America, Inc.
Product code: Code HET
Device class: Class 2
Regulation: 21 CFR 884.1720
Advisory panel: Obstetrics/Gynecology
Date received: 1996-05-14
Decision date: 1996-08-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Melville, NY, US

Download summary PDF View on FDA.gov ↗

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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.