HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-— 510(k) K810625

Name: FDA 510(k) clearance K810625
Creator: U.S. Food and Drug Administration
Published: 1981-03-27

Substantially Equivalent

Serono Laboratories, Inc.

FDA 510(k) clearance K810625 for HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-, Substantially Equivalent on 1981-03-27. Applicant: Serono Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Serono Laboratories, Inc.
Product code: Code DHI
Device class: Class 1
Regulation: 21 CFR 866.5065
Advisory panel: Immunology
Date received: 1981-03-09
Decision date: 1981-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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