CYSTIC FIBROSIS TESTING INSTRUMENT— 510(k) K772176

Name: FDA 510(k) clearance K772176
Creator: U.S. Food and Drug Administration
Published: 1977-12-20

Substantially Equivalent

Laboratory Equipment Design Co.

FDA 510(k) clearance K772176 for CYSTIC FIBROSIS TESTING INSTRUMENT, Substantially Equivalent on 1977-12-20. Applicant: Laboratory Equipment Design Co.. Device class: 1.

Clearance details

Applicant: Laboratory Equipment Design Co.
Product code: Code JJN
Device class: Class 1
Regulation: 21 CFR 862.2485
Advisory panel: Clinical Chemistry
Date received: 1977-11-21
Decision date: 1977-12-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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