Atlas FDA

BIOPROBE FLUOR GENTAMICIN IN SERUM OR PLASMA

FDA 510(k) clearance K852158 · decided 1985-06-25

Clearance details

K-number
K852158
Device name
BIOPROBE FLUOR GENTAMICIN IN SERUM OR PLASMA
Applicant
Bioprobe Intl., Inc.
Decision
Substantially Equivalent
Date received
1985-05-17
Decision date
1985-06-25
Days to decision
39 days
Clearance type
Traditional
Product code
LCQ
Device class
2
Regulation number
862.3450
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Tustin, CA, 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
VARIANT EXPRESS GLYCOHEMOGLOBIN PROGRAM (K972609)Bio-Rad1997-08-06
INNOFLUOR GENTAMICIN ASSAY SYSTEM (K955569)Oxis Intl., Inc.1996-02-09
COBAS(R)-FP REAGENTS FOR GENTAMICIN AND COBAS(R)-FP GENTAMICIN CALIBRATORS (K945523)Roche Diagnostic Systems, Inc.1995-03-09
GENTAMICIN FPIA REAGENT SET AND CALIBRATORS (K943550)Sigma Diagnostics, Inc.1994-11-17
OPUS GENTAMICIN (K905721)Pb Diagnostic Systems, Inc.1991-02-21
'TDXFLX ANALYZER (K904226)Abbott Laboratories1990-10-29
FPR GENTAMICIN KIT (K894523)Colony Laboratories, Inc.1989-09-28
GENTAMICIN KIT(FPIA) (K852013)Windsor Laboratories, Inc.1985-06-10
COBAS REAGENTS FOR GENTAMICIN & CALIBRAT (K843827)Roche Diagnostic Systems, Inc.1985-02-01
INNOFLOUR GENTAMICIN (K841865)Innotron Diagnostics1984-05-31
IMMPULSE GENTAMICIN ASSAY REAGENTS (K841162)Paragon Diagnostics, Inc.1984-05-02
SYVA ADVANCE SYST. EMIT-AMD GENT. ASSAY (K820285)Syva Co.1982-02-18

Recalls involving this device

No recalls on record reference this clearance.