Atlas FDA

GENTAMICIN KIT(FPIA)

FDA 510(k) clearance K852013 · decided 1985-06-10

Clearance details

K-number
K852013
Device name
GENTAMICIN KIT(FPIA)
Applicant
Windsor Laboratories, Inc.
Decision
Substantially Equivalent
Date received
1985-05-09
Decision date
1985-06-10
Days to decision
32 days
Clearance type
Traditional
Product code
LCQ
Device class
2
Regulation number
862.3450
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
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
BIOPROBE FLUOR GENTAMICIN IN SERUM OR PLASMA (K852158)Bioprobe Intl., Inc.1985-06-25
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.