FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

VYNTUS/ SENTRYSUITE PRODUCT LINE

K Number: K133925 · Decision Aug 22, 2014
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
89
Applicant Total
12
Review Days
242

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Basic Information

Device Name
VYNTUS/ SENTRYSUITE PRODUCT LINE
K Number
K133925
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1880
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Carefusion Germany 234 GmbH
Date Received
December 23, 2013
Decision Date
August 22, 2014
Product Code
BZC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
BZC Calculator, Pulmonary Function Data

Similar 510(k) Clearances

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Other Clearances by Carefusion Germany 234 GmbH

K Number Device Name
K153654 Sentry WEB SmartInterp
K150810 Vyntus / SentrySuite Product Line
K142959 Vyntus Walk
K141936 MICROBLAB, MICROLOOP
K122699 SENTRYSUITE PRODUCT LINE
K113813 SENTRYSUITE PRODUCT LINE
K113096 MICRO I
K111408 MICROGARD II
K111053 SENTRYSUITE PRODUCT LINE
K101873 MASTERSCREEN IOS
Search all 12 clearances from Carefusion Germany 234 GmbH →