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

PAP-CHECK RIA KIT

K Number: K792043 · Decision Oct 30, 1979
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
44
Applicant Total
10
Review Days
18

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Basic Information

Device Name
PAP-CHECK RIA KIT
K Number
K792043
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1020
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Serono Laboratories, Inc.
Date Received
October 12, 1979
Decision Date
October 30, 1979
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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K Number Device Name
K834428 ALDOSTERONE RADIOIMMUNOASSAY TEST KIT
K810695 ESTRIOL RADIOIMMUNOASSAY TEST KIT
K810625 HUMAN PLACENTAL LACTOGEN RADIOIMMUNO-
K790679 ESTRADIOL RIA KIT
K790440 PROGESTERONE
K782143 RIA KIT, GLUCOSE
K782103 RIA KIT, NEONATAL T4
K781733 RIA KIT, PREG-STAT
K781285 INSULIN RIA KIT