K771239Substantially Equivalent

Goat Lambda-Light Chain Antihuman Serum

Name: K771239 Goat Lambda-Light Chain Antihuman Serum
Creator: G.D. Searle and Co.
Published: 1977-08-02
License: https://open.fda.gov/license/

G.D. Searle and Co., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K771239 is the FDA 510(k) clearance record for GOAT LAMBDA-LIGHT CHAIN ANTIHUMAN SERUM, cleared for G.D. Searle and Co. on 1977-08-02. FDA records list 56 510(k) clearances for G.D. Searle and Co., from 1976-07-19 to 1982-05-25. As of 2026-09-10, FDA records show no recalls naming K771239.

Clearance record

Decision date: 1977-08-02
Received: 1977-07-11 (22 days to decision)
Review panel: Unknown
Applicant: G.D. Searle and Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No