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
K981232Substantially Equivalent

Ca

Abbott Mfg., Inc., Irving TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981232 is the FDA 510(k) clearance record for CA, a class II device, cleared for Abbott Mfg., Inc. on under FDA product code CJY (Azo Dye, Calcium). FDA records list 14 510(k) clearances for Abbott Mfg., Inc., from to . As of , FDA records show no recalls naming K981232.

Clearance record

Decision date
Received
(45 days to decision)
Product code
CJY Azo Dye, Calcium
Regulation
21 CFR 862.1145
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Abbott Mfg., Inc. 1920 Hurd Dr., Irving TX
510(k) summary
Summary
Third party review
No

Clearances, product code CJY

Trailing 12 months

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

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