510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K963803Substantially Equivalent

Centocor Ca 15-3 Ria Model No. 800-033

Centocor, Inc., Malvern PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K963803 is the FDA 510(k) clearance record for CENTOCOR CA 15-3 RIA MODEL NO. 800-033, a class II device, cleared for Centocor, Inc. on under FDA product code MOI (System, Test, Immunological, Antigen, Tumor). FDA records list 3 510(k) clearances for Centocor, Inc., from to . As of , FDA records show no recalls naming K963803.

Clearance record

Decision date
Received
(242 days to decision)
Product code
MOI System, Test, Immunological, Antigen, Tumor
Regulation
21 CFR 866.6010
Device class
Class II
Review panel
Immunology
Applicant
Centocor, Inc. 200 Great Valley Pkwy., Malvern PA
510(k) summary
Summary
Third party review
No

Clearances, product code MOI

Trailing 12 months

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

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