NML-TETRA-TUBE RIA— 510(k) K823053

Name: FDA 510(k) clearance K823053
Creator: U.S. Food and Drug Administration
Published: 1982-11-10

Substantially Equivalent

Nuclear Medical Laboratories, Inc.

FDA 510(k) clearance K823053 for NML-TETRA-TUBE RIA, Substantially Equivalent on 1982-11-10. Applicant: Nuclear Medical Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Nuclear Medical Laboratories, Inc.
Product code: Code CDX
Device class: Class 2
Regulation: 21 CFR 862.1700
Advisory panel: Clinical Chemistry
Date received: 1982-10-18
Decision date: 1982-11-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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