AQUAMATIC K-MODULE MODEL K-10— 510(k) K761337

Name: FDA 510(k) clearance K761337
Creator: U.S. Food and Drug Administration
Published: 1977-01-10

Substantially Equivalent

Gorman Rupp Industries

FDA 510(k) clearance K761337 for AQUAMATIC K-MODULE MODEL K-10, Substantially Equivalent on 1977-01-10. Applicant: Gorman Rupp Industries. Device class: 1.

Clearance details

Applicant: Gorman Rupp Industries
Product code: Code JRR
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1976-12-27
Decision date: 1977-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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