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

SERALYZER(R) THERAPEUTIC DRUG ASSAY CONTROL(ABNOR)

K Number: K921939 · Decision Jul 16, 1992
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
82
Applicant Total
145
Review Days
83

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Basic Information

Device Name
SERALYZER(R) THERAPEUTIC DRUG ASSAY CONTROL(ABNOR)
K Number
K921939
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Heraeus Kulzer, Inc.
Date Received
April 24, 1992
Decision Date
July 16, 1992
Product Code
LAS
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
LAS Drug Specific Control Materials

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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. →