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

BIPAP SYNCHRONY 2 VENTILATORY SUPPORT SYSTEM

K Number: K071509 · Decision Aug 8, 2007
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
46
Applicant Total
21
Review Days
65

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Basic Information

Device Name
BIPAP SYNCHRONY 2 VENTILATORY SUPPORT SYSTEM
K Number
K071509
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.5895
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Respironics Inc., Sleep & Home Respiratory Group
Date Received
June 4, 2007
Decision Date
August 8, 2007
Product Code
MNS
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
MNS Ventilator, Continuous, Non-Life-Supporting

Similar 510(k) Clearances

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

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Other Clearances by Respironics Inc., Sleep & Home Respiratory Group

K Number Device Name
K092835 COMFORTGEL NASAL MASK
K092648 RESPIRONICS PERFORMAX SE TOTAL FACE MASK
K090539 BIPAP AUTOSV ADVANCED
K091191 GAS TRANSFILL
K091843 COMFORT TWIN NASAL MASK
K091066 COMFORT TWIN NASAL MASK
K091319 REMSTAR AUTO A-FLEX
K090484 ALICE PDX
K091271 RESPIRONICS PERFORMAX TOTAL FACE MASK
K090243 REMSTAR M-SERIES AUTO WITH AFLEX CPAP SYSTEM
Search all 21 clearances from Respironics Inc., Sleep & Home Respiratory Group →