Atlas FDA

FIAX TEST KIT FOR TOBRAMYCIN QUANTITA

FDA 510(k) clearance K801308 · decided 1980-06-20

Clearance details

K-number
K801308
Device name
FIAX TEST KIT FOR TOBRAMYCIN QUANTITA
Applicant
Intl. Diagnostic Technology
Decision
Substantially Equivalent
Date received
1980-06-03
Decision date
1980-06-20
Days to decision
17 days
Clearance type
Traditional
Product code
LCR
Device class
2
Regulation number
862.3900
Medical specialty
Clinical Toxicology
Advisory committee
Clinical Toxicology
Location
Mchenry, IL, 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
QMS TOBRAMYCIN (K060998)Seradyn, Inc.2006-07-21
ACS TOBRAMYCIN (K974029)Chiron Diagnostics Corp.1998-02-12
TOBRAMYCIN FLEX REAGENT CARTRIDGE (K962818)Dade Intl., Inc.1996-09-13
BECKMAN ARRAY TOBRAMYCIN (TOB) REAGENT (K952568)Beckman Instruments, Inc.1995-08-08
OPUS(R) TOBRAMYCIN (K911940)Pb Diagnostic Systems, Inc.1991-07-01
VAR AURAL GROM AG/S9,SD8.00.28.5/0.2 NS/S/6823 1.4 (K911613)Exmoor Plastics , Ltd.1991-06-28
INTRAOCULAR PRESSURE REDUCER (K854873)Mira, Inc.1986-02-04
DU PONT TOBRAMYCIN ASSAY REAGENTS (K850058)E.I. Dupont DE Nemours & Co., Inc.1985-01-18
IMMPULSE TOBRAMYCIN ASSAY REAGENTS (K840847)Paragon Diagnostics, Inc.1984-04-04
STRATUS TOBRAMYCIN FLUOROMETRIC ENZYM (K832408)American Dade1983-08-26
NEEDLE HOLDERS (K822197)Kelleher Corp.1982-08-16
VIRGO IMMUNO-PRECIPITATION ASSAY TOBRA (K821542)Electro-Nucleonics Laboratories, Inc.1982-06-03

Recalls involving this device

No recalls on record reference this clearance.