FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

INNOTRON FLUORIMETER SERIES ONE-10

K Number: K822942 · Decision Dec 9, 1982
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
37
Applicant Total
28
Review Days
66

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Basic Information

Device Name
INNOTRON FLUORIMETER SERIES ONE-10
K Number
K822942
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2560
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Innotron of Oregon, Inc.
Date Received
October 4, 1982
Decision Date
December 9, 1982
Product Code
KHO
Advisory Committee
Clinical Chemistry
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
KHO Fluorometer, For Clinical Use

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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. →