MODIFICATION TO API UNISCEPT 20GP— 510(k) K901559

Name: FDA 510(k) clearance K901559
Creator: U.S. Food and Drug Administration
Published: 1990-09-10

Substantially Equivalent

Analytical Products, Inc.

FDA 510(k) clearance K901559 for MODIFICATION TO API UNISCEPT 20GP, Substantially Equivalent on 1990-09-10. Applicant: Analytical Products, Inc.. Device class: 1.

Clearance details

Applicant: Analytical Products, Inc.
Product code: Code LQL
Device class: Class 1
Regulation: 21 CFR 866.2660
Advisory panel: Microbiology
Date received: 1990-04-03
Decision date: 1990-09-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Plainview, NY, US

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