Medical Device
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K963251Substantially Equivalent

Ciba Corning Acs;180 Dpd Assay

Ciba Corning Diagnostics Corp., Irvine CA / Traditional, Substantially Equivalent

K963251 is the FDA 510(k) clearance record for CIBA CORNING ACS;180 DPD ASSAY, a class I device, cleared for Ciba Corning Diagnostics Corp. on under FDA product code JMM (Column Chromatography & Color Development, Hydroxyproline). FDA records list 125 510(k) clearances for Ciba Corning Diagnostics Corp., from to . As of , FDA records show no recalls naming K963251.

Clearance record

Decision date
Received
(57 days to decision)
Product code
JMM Column Chromatography & Color Development, Hydroxyproline
Regulation
21 CFR 862.1400
Device class
Class I
Review panel
Clinical Chemistry
Applicant
Ciba Corning Diagnostics Corp. 17392 Daimler St., Irvine CA
510(k) summary
Summary
Third party review
No

Clearances, product code JMM

Trailing 12 months

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

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