Atlas FDA

OPUS PHENYTOIN TEST SYSTEM

FDA 510(k) clearance K896868 · decided 1990-01-02

Clearance details

K-number
K896868
Device name
OPUS PHENYTOIN TEST SYSTEM
Applicant
Pb Diagnostic Systems, Inc.
Decision
Substantially Equivalent
Date received
1989-12-07
Decision date
1990-01-02
Days to decision
26 days
Clearance type
Traditional
Product code
LGR
Device class
2
Regulation number
862.3350
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Westwood, MA, 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
ACS PHENYTOIN ASSAY (K955873)Ciba Corning Diagnostics Corp.1996-03-11
INNOFLUOR PHENYTOIN ASSAY SYSTEM (K955562)Oxis Intl., Inc.1996-01-24
AXSYM PHENYTOIN II (K953840)Abbott Laboratories1995-09-25
TDX(R)/TDXFLX(R) PHENYTOIN II (K946328)Abbott Laboratories1995-03-28
PHENYTOIN FPIA REAGENT SET AND CALIBRATORS (K943313)Sigma Diagnostics, Inc.1994-10-27
AXSYM PHENYTOIN ASSAY (K935375)Abbott Laboratories1994-06-21
COBAS-FP REAGENT FOR PHENYTOIN AND COBA-FP PHENYTOIN CALIBRATORS (K936131)Roche Diagnostic Systems, Inc.1994-03-11
INNOFLUOR PHENYTOIN MANUAL FPIA REAGENT SET (K895827)Innotron of Oregon, Inc.1989-10-31
INNOTRON INNOFLUOR PHEYTOIN REAGENT SET (K872563)Innotron of Oregon, Inc.1987-08-21
IMMPULSE PHENYTOIN ASSAY REAGENT (K862554)Sclavo, Inc.1986-07-16
COBAS FP REAGENTS FOR PHENYTOIN & CALIBR (K843824)Roche Diagnostic Systems, Inc.1985-02-01
PHENYTOIN RADIOIMMUNOASSAY USING THE ARIA HT SYSTE (K844171)Bd Becton Dickinson Vacutainer Systems Preanalytic1984-12-10

Recalls involving this device

No recalls on record reference this clearance.