Atlas FDA

INVENT SNORING DEVICE

FDA 510(k) clearance K120665 · decided 2012-06-12

Clearance details

K-number
K120665
Device name
INVENT SNORING DEVICE
Applicant
Ventus Medical, Inc.
Decision
Substantially Equivalent
Date received
2012-03-05
Decision date
2012-06-12
Days to decision
99 days
Clearance type
Traditional
Product code
LWF
Device class
1
Regulation number
874.3900
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Hillsborough, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.