Atlas FDA

PHENOBARBITAL-FPIA FLUORES. POLAR. IMMUNOASSAY KIT

FDA 510(k) clearance K863625 · decided 1986-11-10

Clearance details

K-number
K863625
Device name
PHENOBARBITAL-FPIA FLUORES. POLAR. IMMUNOASSAY KIT
Applicant
Windsor Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1986-09-17
Decision date
1986-11-10
Days to decision
54 days
Clearance type
Traditional
Product code
LGQ
Device class
2
Regulation number
862.3660
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Garland, TX, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
INNOFLUOR GENTAMICIN ASSAY SYSTEM (K972331)Oxis Intl., Inc.1997-08-01
INNOFLUOR PHENOBARBITAL ASSAY SYSTEM (K972330)Oxis Intl., Inc.1997-07-14
AXSYM PHENOBARBITAL (K940596)Abbott Laboratories1994-06-21
COBAS-FP REAGENT FOR PHENOBARBITAL AND COBAS-FP PHENOBARBITAL CALIBRATORS (K936130)Roche Diagnostic Systems, Inc.1994-03-11
MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA (K900704)Innotron of Oregon, Inc.1990-04-12
FPR PHENOBARBITAL KIT (K894525)Colony Laboratories, Inc.1989-08-28
COBAS FP REAGENTS FOR PHENO & COBAS FP PHENO CALI. (K872397)Roche Diagnostic Systems, Inc.1987-07-21
IMMPULSE PHENOBARBITAL ASSAY REAGENTS (K862528)Sclavo, Inc.1986-07-16
TDX BARBITURATES (K854044)Abbott Laboratories1985-10-28
COBAS REAGENTS PHENOBARBITAL & PHENOBAR (K843825)Roche Diagnostic Systems, Inc.1985-02-01
INNOFLUOR PHENOBARBITAL (K841707)Innotron Diagnostics1984-05-23

Recalls involving this device

No recalls on record reference this clearance.