FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

INNOTRON INNOFLUOR TOBRAMYCIN REAGENT SET

K Number: K872562 · Decision Aug 17, 1987
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
9
Applicant Total
28
Review Days
54

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Basic Information

Device Name
INNOTRON INNOFLUOR TOBRAMYCIN REAGENT SET
K Number
K872562
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3900
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Innotron of Oregon, Inc.
Date Received
June 24, 1987
Decision Date
August 17, 1987
Product Code
LFW
Advisory Committee
Clinical Toxicology
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LFW Fluorescence Polarization Immunoassay, Tobramycin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LFW), ordered by most recent decision date.

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Other Clearances by Innotron of Oregon, Inc.

K Number Device Name
K903101 INNOFLUOR (TM) AMIKACIN CALIBRATOR SET
K903100 INNOFLUOR (TM) AMIKACIN REAGENT SET
K900707 MODIFIED ACCUFLUOR TOBRAMYCIN REAGENT & CALIBRATOR
K900708 MODIFIED ACCUFLUOR VANCOMYCIN REAGENT & CALIBRATOR
K900704 MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA
K900703 MODIFIED ACCUFLUOR GENTAMICIN REAGENT & CALIBRATOR
K900705 MODIFIED ACCUFLUOR QUINIDINE REAGENT & CALIBRATOR
K900706 MODIFIED ACCUFLUOR THEOPHYLLINE REAGENT & CALIBRA
K900702 MODIFIED ACCUFLUOR CARBAMAZEPINE REAGENT & CALIBRA
K895827 INNOFLUOR PHENYTOIN MANUAL FPIA REAGENT SET
Search all 28 clearances from Innotron of Oregon, Inc. →