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

CLINISTAT POTASSIUM REAGENT TEST

K Number: K895047 · Decision Oct 17, 1989
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
20
Applicant Total
145
Review Days
69

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Basic Information

Device Name
CLINISTAT POTASSIUM REAGENT TEST
K Number
K895047
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1410
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Heraeus Kulzer, Inc.
Date Received
August 9, 1989
Decision Date
October 17, 1989
Product Code
CFM
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
CFM Bathophenanthroline, Colorimetry, Iron (Non-Heme)

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Other Clearances by Heraeus Kulzer, Inc.

K Number Device Name
K091494 FLEXITIME FLOW
K063062 HKBOND 2006
K060994 MONDIAL
K052543 HERACERAM ZIRKONIA
K043504 PALAIMPACT
K043295 VERSYO.DIRECT
K042878 FLEXITIME XTREME
K030052 OSTIM
K040859 HERACERAM PRESS
K040043 NDX-40 ALLOY
Search all 145 clearances from Heraeus Kulzer, Inc. →