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

TECHNICON H* 3 RTX SYSTEM (IN-VITRO DIAG. SYSTEM)

K Number: K930148 · Decision May 11, 1993
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
379
Applicant Total
145
Review Days
119

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Basic Information

Device Name
TECHNICON H* 3 RTX SYSTEM (IN-VITRO DIAG. SYSTEM)
K Number
K930148
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.5220
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
January 12, 1993
Decision Date
May 11, 1993
Product Code
GKZ
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
GKZ Counter, Differential Cell

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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. →