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

CLEAN PEAK FLOW METER

K Number: K091412 · Decision Aug 21, 2009
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
79
Applicant Total
14
Review Days
100

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Basic Information

Device Name
CLEAN PEAK FLOW METER
K Number
K091412
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.1860
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Viasys Healthcare GmbH
Date Received
May 13, 2009
Decision Date
August 21, 2009
Product Code
BZH
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
BZH Meter, Peak Flow, Spirometry

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Other Clearances by Viasys Healthcare GmbH

K Number Device Name
K092324 SPIROPRO
K091505 COR12+
K081823 MASTERSCREEN PAED - BABY BODY
K080510 VIP PULMONARY FUNCTION SYSTEM
K080734 FLOWSCREEN, FLOWSCREEN/CORSCREEN, FLOWSCREEN CT
K072061 MASTERSCREEN PFT, MASTERSCREEN PFT CT, MASTERSCREEN PFT BODY
K072323 MASTERSCREEN & OXYCON CPX
K071753 MASTERSCREEN PNEUMO & MASTERSCOPE
K062011 MODIFICATION TO FLOWSCREEN
K070614 CORSCREEN
Search all 14 clearances from Viasys Healthcare GmbH →