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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| ACUTEK'S CLEARPASAGE (K962698) | Acutek Adhesive Specialties, Inc. | 1996-09-09 |
| BREATHE RIGHT NASAL STRIP (K955711) | Cns, Inc. | 1996-05-30 |
| BREATHE RIGHT NASAL STRIP (K954914) | Cns, Inc. | 1996-02-27 |
| EASY BREATHING NASAL STRIPS (K955233) | Corbett Lair, Inc. | 1995-12-21 |
| E-Z BREATHERS (K953042) | E-Z Kare Good Health Systems, Inc. | 1995-12-08 |
| BURGET NASAL STENT (K942025) | Bivona Medical Technologies | 1995-10-27 |
| BREATHE RIGHT NASAL STRIP (K953772) | Cns, Inc. | 1995-10-20 |
Recalls involving this device
No recalls on record reference this clearance.