TITERTEK MICROPLATE INCUBATOR— 510(k) K812340

Name: FDA 510(k) clearance K812340
Creator: U.S. Food and Drug Administration
Published: 1981-09-23

Substantially Equivalent

Flow Laboratories, Inc.

FDA 510(k) clearance K812340 for TITERTEK MICROPLATE INCUBATOR, Substantially Equivalent on 1981-09-23. Applicant: Flow Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Flow Laboratories, Inc.
Product code: Code JTQ
Device class: Class 1
Regulation: 21 CFR 866.2540
Advisory panel: Microbiology
Date received: 1981-08-18
Decision date: 1981-09-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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