QUICK CEPT— 510(k) K801668

Substantially Equivalent

Laboratory Diagnostics Co., Inc.

FDA 510(k) clearance K801668 for QUICK CEPT, Substantially Equivalent on 1980-08-13. Applicant: Laboratory Diagnostics Co., Inc.. Device class: 2.

Clearance details

Applicant: Laboratory Diagnostics Co., Inc.
Product code: Code JHS
Device class: Class 2
Regulation: 21 CFR 862.1215
Advisory panel: Clinical Chemistry
Date received: 1980-07-21
Decision date: 1980-08-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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