510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K772077Substantially Equivalent

Radial Immunodiffusion Kit-Immunoglob.g

Gelman Instrument Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K772077 is the FDA 510(k) clearance record for RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.G, a class II device, cleared for Gelman Instrument Co. on under FDA product code DEW (Igg, Antigen, Antiserum, Control). FDA records list 11 510(k) clearances for Gelman Instrument Co., from to . As of , FDA records show no recalls naming K772077.

Clearance record

Decision date
Received
(92 days to decision)
Product code
DEW Igg, Antigen, Antiserum, Control
Regulation
21 CFR 866.5510
Device class
Class II
Review panel
Immunology
Applicant
Gelman Instrument Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code DEW

Trailing 12 months

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

FDA records show no clearances under product code DEW in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DEW, 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