FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CIBA CORNING MAGIC LITE PROLACTIN IMMUNOASSAY

K Number: K894988 · Decision Oct 12, 1989
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
79
Applicant Total
125
Review Days
65

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CIBA CORNING MAGIC LITE PROLACTIN IMMUNOASSAY
K Number
K894988
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1625
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Ciba Corning Diagnostics Corp.
Date Received
August 8, 1989
Decision Date
October 12, 1989
Product Code
CFT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CFT Radioimmunoassay, Prolactin (Lactogen)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CFT), ordered by most recent decision date.

View all

Other Clearances by Ciba Corning Diagnostics Corp.

K Number Device Name
K962559 ACS CORTISOL IMMUNOASSAY
K963251 CIBA CORNING ACS;180 DPD ASSAY
K961807 CERTAIN HCT LEVEL A & LEVEL B/CVM HCT LEVELS 1,2,3, & 4
K961657 CIBA CORNING 400 SYSTEM
K962021 CIBA CORNING 348 SYSTEM
K962126 ACS CKMB II IMMUNOASSAY
K962041 ACS LH2 IMMUNOASSAY
K961510 ACS FRT4 IMMUNOASSAY
K960246 LIQUID CARDIAC MARKER 1,2,3 ASSAYED
K955873 ACS PHENYTOIN ASSAY
Search all 125 clearances from Ciba Corning Diagnostics Corp. →