510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772003Substantially Equivalent

Human Reference Serum C4 Complement

G.D. Searle and Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772003 is the FDA 510(k) clearance record for HUMAN REFERENCE SERUM C4 COMPLEMENT, a class II device, cleared for G.D. Searle and Co. on under FDA product code DAK (Complement C1q, Antigen, Antiserum, Control). FDA records list 56 510(k) clearances for G.D. Searle and Co., from to . As of , FDA records show no recalls naming K772003.

Clearance record

Decision date
Received
(13 days to decision)
Product code
DAK Complement C1q, Antigen, Antiserum, Control
Regulation
21 CFR 866.5240
Device class
Class II
Review panel
Immunology
Applicant
G.D. Searle and Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DAK

Trailing 12 months

FDA records hold no clearances under product code DAK in the trailing twelve months.

FDA records show no clearances under product code DAK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DAK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260