ACCUPROBE STREPTOCOCCUS PNEUMONIAE CULTURE CONFIR.— 510(k) K902908

Name: FDA 510(k) clearance K902908
Creator: U.S. Food and Drug Administration
Published: 1990-08-06

Substantially Equivalent

Gen-Probe, Inc.

FDA 510(k) clearance K902908 for ACCUPROBE STREPTOCOCCUS PNEUMONIAE CULTURE CONFIR., Substantially Equivalent on 1990-08-06. Applicant: Gen-Probe, Inc.. Device class: 1.

Clearance details

Applicant: Gen-Probe, Inc.
Product code: Code MCT
Device class: Class 1
Regulation: 21 CFR 866.3740
Advisory panel: Microbiology
Date received: 1990-07-02
Decision date: 1990-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

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