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

SERALYZER DIGOXIN ASSAY/TEST MOD/CALIB/CONTR/AMES

K Number: K884528 · Decision Mar 8, 1989
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
84
Applicant Total
145
Review Days
131

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Basic Information

Device Name
SERALYZER DIGOXIN ASSAY/TEST MOD/CALIB/CONTR/AMES
K Number
K884528
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3320
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Heraeus Kulzer, Inc.
Date Received
October 28, 1988
Decision Date
March 8, 1989
Product Code
KXT
Advisory Committee
Clinical Toxicology
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
KXT Enzyme Immunoassay, Digoxin

Similar 510(k) Clearances

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

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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. →