FIBER OPTIC ENDOILLUMINATION PROBE— 510(k) K982462

Name: FDA 510(k) clearance K982462
Creator: U.S. Food and Drug Administration
Published: 1998-09-14

Substantially Equivalent

Microvision, Inc.

FDA 510(k) clearance K982462 for FIBER OPTIC ENDOILLUMINATION PROBE, Substantially Equivalent on 1998-09-14. Applicant: Microvision, Inc.. Device class: 2.

Clearance details

Applicant: Microvision, Inc.
Product code: Code FFS
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1998-07-15
Decision date: 1998-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seabrook, NH, US

Download summary PDF View on FDA.gov ↗

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