Atlas FDA

ROCHE COBAS-FP REAGENTS FOR TOBRAMYCIN

FDA 510(k) clearance K964670 · decided 1997-02-04

Clearance details

K-number
K964670
Device name
ROCHE COBAS-FP REAGENTS FOR TOBRAMYCIN
Applicant
Roche Diagnostic Systems, Inc.
Decision
Substantially Equivalent
Date received
1996-11-21
Decision date
1997-02-04
Days to decision
75 days
Clearance type
Traditional
Product code
LFW
Device class
2
Regulation number
862.3900
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Somerville, NJ, 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
TOBRAMYCIN FPIA REAGENT SET AND CALIBRATOR (K944371)Sigma Diagnostics, Inc.1994-11-10
AXSYM TOBRAMYCIN (K941614)Abbott Laboratories1994-08-18
CEDIA(R) TOBRAMYCIN ASSAY (K912143)Microgenics Corp.1991-07-26
MODIFIED ACCUFLUOR TOBRAMYCIN REAGENT & CALIBRATOR (K900707)Innotron of Oregon, Inc.1990-04-20
FPR TOBRAMYCIN KIT (K894531)Colony Laboratories, Inc.1989-09-01
INNOTRON INNOFLUOR TOBRAMYCIN REAGENT SET (K872562)Innotron of Oregon, Inc.1987-08-17
TOBRAMYCIN KIT(FPIA)FLUORESCENCE POLARIZATION IMMU (K854392)Windsor Laboratories, Inc.1985-12-05
COBAS REAGENTS FOR TOBRAMYCIN & CALIBRA (K843828)Roche Diagnostic Systems, Inc.1985-02-01
INNOFLOUR TOBRAMYCIN (K841866)Innotron Diagnostics1984-05-31

Recalls involving this device

No recalls on record reference this clearance.