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

CARBAMAZEPINE (FPIA) CALIBRATOR KIT

K Number: K873281 · Decision Oct 28, 1987
Classifications
1
FEI Numbers
40
Registration Numbers
40
Same Product Code
122
Applicant Total
19
Review Days
72

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Basic Information

Device Name
CARBAMAZEPINE (FPIA) CALIBRATOR KIT
K Number
K873281
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3200
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Windsor Laboratories, Inc.
Date Received
August 17, 1987
Decision Date
October 28, 1987
Product Code
DLJ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DLJ Calibrators, Drug Specific

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Other Clearances by Windsor Laboratories, Inc.

K Number Device Name
K873282 CARBAMAZEPINE FPIA FLUORES. POLARIZA. IMMUNOASSAY
K871486 (FPIA) ASSAY BUFFER
K870389 DIGOXIN (FPIA) CALIBRATOR KIT
K870390 PHENOBARBITAL (FPIA) CALIBRATOR KIT
K864333 DIGOXIN FPIA FLUORESCENCE POLARIZATION IMMUNOASSAY
K863625 PHENOBARBITAL-FPIA FLUORES. POLAR. IMMUNOASSAY KIT
K863244 AMIKACIN (FPIA) CALIBRATOR KIT
K862248 AMIKACIN KIT (FPIA)
K861770 PHENYTOIN (FPIA) CALIBRATOR KIT
K861768 THEOPHYLLINE (FPIA) CALIBRATOR KIT
Search all 19 clearances from Windsor Laboratories, Inc. →