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

CLINITEK ATLAS AUTOMATED URINE CHEMISTRY ANALYZER

K Number: K946183 · Decision Feb 22, 1995
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
45
Applicant Total
145
Review Days
64

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CLINITEK ATLAS AUTOMATED URINE CHEMISTRY ANALYZER
K Number
K946183
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2900
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
December 20, 1994
Decision Date
February 22, 1995
Product Code
KQO
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
KQO Automated Urinalysis System

Similar 510(k) Clearances

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

View all

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. →