SCOPEJOCKEY— 510(k) K940780

Substantially Equivalent

Fibertech Instruments, Inc.

FDA 510(k) clearance K940780 for SCOPEJOCKEY, Substantially Equivalent on 1994-05-10. Applicant: Fibertech Instruments, Inc.. Device class: 2.

Clearance details

Applicant: Fibertech Instruments, Inc.
Product code: Code OCU
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1994-02-22
Decision date: 1994-05-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baltimore, MD, US

Download summary PDF View on FDA.gov ↗

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