FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TANDEM(R) M-PAK(TM) PAP IMMUNOENZYMETRIC ASSAY

K Number: K864945 · Decision Jan 5, 1987
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
44
Applicant Total
63
Review Days
19

Basic Information

Device Name
TANDEM(R) M-PAK(TM) PAP IMMUNOENZYMETRIC ASSAY
K Number
K864945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1020
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
HYBRITECH, INC.
Date Received
December 17, 1986
Decision Date
January 5, 1987
Product Code
JFH
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
JFH Acid Phosphatase (Prostatic), Tartrate Inhibited

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