PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT— 510(k) K810506

Name: FDA 510(k) clearance K810506
Creator: U.S. Food and Drug Administration
Published: 1981-04-07

Substantially Equivalent

Propper Mfg. Co., Inc.

FDA 510(k) clearance K810506 for PROPPER SIGMOIDOSCOPE SUCTION INSTRUMENT, Substantially Equivalent on 1981-04-07. Applicant: Propper Mfg. Co., Inc.. Device class: 2.

Clearance details

Applicant: Propper Mfg. Co., Inc.
Product code: Code OCX
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1981-02-24
Decision date: 1981-04-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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