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

SLEEPWEAVER NASAL CPAP MASK

K Number: K092362 · Decision Nov 2, 2009
Classifications
1
FEI Numbers
118
Registration Numbers
118
Same Product Code
459
Applicant Total
5
Review Days
90

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Basic Information

Device Name
SLEEPWEAVER NASAL CPAP MASK
K Number
K092362
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5905
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Circadiance, LLC
Date Received
August 4, 2009
Decision Date
November 2, 2009
Product Code
BZD
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
BZD Ventilator, Non-Continuous (Respirator)

Similar 510(k) Clearances

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

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Other Clearances by Circadiance, LLC

K Number Device Name
K162905 SleepWeaver 3D Nasal Mask
K151683 SleepWeaver Advance Pediatric Nasal CPAP Mask
K130481 SLEEPWEAVER ANEW FULL FACE SOFT CLOTH PAP MASK
K120757 SLEEPWEAVER ELAN NASAL CPAP MASK