PHADEBACT HAEMOPHILUS TEST— 510(k) K802423

Substantially Equivalent

Pharmacia, Inc.

FDA 510(k) clearance K802423 for PHADEBACT HAEMOPHILUS TEST, Substantially Equivalent on 1980-11-12. Applicant: Pharmacia, Inc.. Device class: 2.

Clearance details

Applicant: Pharmacia, Inc.
Product code: Code GRO
Device class: Class 2
Regulation: 21 CFR 866.3300
Advisory panel: Microbiology
Date received: 1980-10-03
Decision date: 1980-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.