CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS— 510(k) K893499

Name: FDA 510(k) clearance K893499
Creator: U.S. Food and Drug Administration
Published: 1989-11-16

Substantially Equivalent

Cmsi

FDA 510(k) clearance K893499 for CMS FAST CUT, CMS DIAMOND AND CMS WIRE PASS, Substantially Equivalent on 1989-11-16. Applicant: Cmsi. Device class: 1.

Clearance details

Applicant: Cmsi
Product code: Code EQJ
Device class: Class 1
Regulation: 21 CFR 874.4140
Advisory panel: Ear, Nose, Throat
Date received: 1989-05-04
Decision date: 1989-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: South Bend, IN, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code EQJ

product code EQJ

Malfunction: 1,552
Total: 1,552

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.