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

NAPHTHYL PHOSPHATE, ACID PHOSPHATASE

K Number: K863832 · Decision Dec 16, 1986
Classifications
1
FEI Numbers
9
Registration Numbers
9
Same Product Code
44
Applicant Total
74
Review Days
77

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
NAPHTHYL PHOSPHATE, ACID PHOSPHATASE
K Number
K863832
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1020
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Pointe Scientific, Inc.,
Date Received
September 30, 1986
Decision Date
December 16, 1986
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

Similar 510(k) Clearances

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

View all

Other Clearances by Pointe Scientific, Inc.,

K Number Device Name
K070757 MICROPROTEIN REAGENT SET
K062118 POINTE 360
K070251 CARBON DIOXIDE LIQUID STABLE REAGENT
K070207 MULTI-ANALYTE CHEMISTRY CALIBRATOR
K070504 AMMONIA/ALCOHOL CONTROL SET
K061377 APOLIPOPROTEIN A1 AND APOLIPOPROTEIN B REAGENTS AND CALIBRATORS
K051646 ISE DILUENT, 1N KCL, INTERNAL REFERENCE AND ISE STANDARDS LOW AND HIGH
K040391 TOTAL BILIRUBIN REAGENT SET
K031539 HEMOGLOBIN A1C REAGENT SET
K023860 MICROALBUMIN REAGENT SET AND CALIBRATORS
Search all 74 clearances from Pointe Scientific, Inc., →