Atlas FDA

CENTOCOR CA 15-3 RIA MODEL NO. 800-033

FDA 510(k) clearance K963803 · decided 1997-05-23

Clearance details

K-number
K963803
Device name
CENTOCOR CA 15-3 RIA MODEL NO. 800-033
Applicant
Centocor, Inc.
Decision
Substantially Equivalent
Date received
1996-09-23
Decision date
1997-05-23
Days to decision
242 days
Clearance type
Traditional
Product code
MOI
Device class
2
Regulation number
866.6010
Medical specialty
Immunology
Advisory committee
Immunology
Location
Malvern, PA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
CA 125 ANTIBODY RIA (P850009/S007)Centocor, Inc.1994-12-21
CA 125 ANTIBODY RIA (P850009/S006)Centocor, Inc.1994-03-23
CA 125 ANTIBODY RIA (P850009/S005)Centocor, Inc.1992-07-15
CA 125 ANTIBODY RIA (P850009/S004)Centocor, Inc.1991-03-28
CA 125 ANTIBODY RIA (P850009/S002)Centocor, Inc.1990-02-13
CA 125 ANTIBODY RIA (P850009/S001)Centocor, Inc.1987-07-28