MOUSE LIVER KIDNEY STOMACH DIAGNOSTIC TEST KIT— 510(k) K971658

Name: FDA 510(k) clearance K971658
Creator: U.S. Food and Drug Administration
Published: 1997-05-23

Substantially Equivalent

Jay H. Geller

FDA 510(k) clearance K971658 for MOUSE LIVER KIDNEY STOMACH DIAGNOSTIC TEST KIT, Substantially Equivalent on 1997-05-23. Applicant: Jay H. Geller. Device class: 2.

Clearance details

Applicant: Jay H. Geller
Product code: Code DBL
Device class: Class 2
Regulation: 21 CFR 866.5660
Advisory panel: Immunology
Date received: 1997-04-14
Decision date: 1997-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Santa Monica, CA, US

Download summary PDF View on FDA.gov ↗

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