510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K812727Substantially Equivalent

Gastrin 1-17 by Radioimmunoassay Kit

Immuno Nuclear Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K812727 is the FDA 510(k) clearance record for GASTRIN 1-17 BY RADIOIMMUNOASSAY KIT, a class I device, cleared for Immuno Nuclear Corp. on under FDA product code CGC (Radioimmunoassay, Gastrin). FDA records list 30 510(k) clearances for Immuno Nuclear Corp., from to . As of , FDA records show no recalls naming K812727.

Clearance record

Decision date
Received
(38 days to decision)
Product code
CGC Radioimmunoassay, Gastrin
Regulation
21 CFR 862.1325
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Immuno Nuclear Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code CGC

Trailing 12 months

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

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