ROBINSON KIT - 750014 & 750016— 510(k) K772342

Name: FDA 510(k) clearance K772342
Creator: U.S. Food and Drug Administration
Published: 1978-02-24

Substantially Equivalent

Latex Ind., Inc.

FDA 510(k) clearance K772342 for ROBINSON KIT - 750014 & 750016, Substantially Equivalent on 1978-02-24. Applicant: Latex Ind., Inc.. Device class: 2.

Clearance details

Applicant: Latex Ind., Inc.
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1977-12-22
Decision date: 1978-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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