KEMTEK 102— 510(k) K830751

Substantially Equivalent

Kemble Instruments, Inc.

FDA 510(k) clearance K830751 for KEMTEK 102, Substantially Equivalent on 1983-04-06. Applicant: Kemble Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Kemble Instruments, Inc.
Product code: Code JJJ
Device class: Class 1
Regulation: 21 CFR 862.2320
Advisory panel: Clinical Chemistry
Date received: 1983-03-10
Decision date: 1983-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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