TANDEM-M IMMUNOENZYMETRIC ASSAY FOR PROLACTIN— 510(k) K863860

Name: FDA 510(k) clearance K863860
Creator: U.S. Food and Drug Administration
Published: 1986-11-21

Substantially Equivalent

Hybritech, Inc.

FDA 510(k) clearance K863860 for TANDEM-M IMMUNOENZYMETRIC ASSAY FOR PROLACTIN, Substantially Equivalent on 1986-11-21. Applicant: Hybritech, Inc.. Device class: 1.

Clearance details

Applicant: Hybritech, Inc.
Product code: Code CFT
Device class: Class 1
Regulation: 21 CFR 862.1625
Advisory panel: Clinical Chemistry
Date received: 1986-10-03
Decision date: 1986-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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