MUELLER HINTON AGAR WITH 2% NACI— 510(k) K960313

Substantially Equivalent

Remel, L.P.

FDA 510(k) clearance K960313 for MUELLER HINTON AGAR WITH 2% NACI, Substantially Equivalent on 1996-03-25. Applicant: Remel, L.P.. Device class: 2.

Clearance details

Applicant: Remel, L.P.
Product code: Code JTZ
Device class: Class 2
Regulation: 21 CFR 866.1700
Advisory panel: Microbiology
Date received: 1996-01-22
Decision date: 1996-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lenexa, KS, US

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