FIBER OPTICS PROCTOSCOPE— 510(k) K771920

Name: FDA 510(k) clearance K771920
Creator: U.S. Food and Drug Administration
Published: 1977-10-20

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K771920 for FIBER OPTICS PROCTOSCOPE, Substantially Equivalent on 1977-10-20. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Code GCP
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1977-10-12
Decision date: 1977-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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