FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Bongo
K Number: K180619
·
Decision Aug 16, 2018
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
4
Applicant Total
1
Review Days
160
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Basic Information
- Device Name
- Bongo
- K Number
- K180619
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 872.5570
- Medical Specialty
- Dental
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Innomed Healthscience, Inc.
- Date Received
- March 9, 2018
- Decision Date
- August 16, 2018
- Product Code
- OHP
- Advisory Committee
- Dental
- Review Advisory Committee
- EN
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OHP | Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea | FDA class 2 | Dental |
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