FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PeriView FLEX
K Number: K171232
·
Decision Sep 21, 2017
Classifications
1
FEI Numbers
54
Registration Numbers
54
Same Product Code
27
Applicant Total
8
Review Days
147
Basic Information
- Device Name
- PeriView FLEX
- K Number
- K171232
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.4680
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Olympus Surgical Technologies America
- Date Received
- April 27, 2017
- Decision Date
- September 21, 2017
- Product Code
- KTI
- Advisory Committee
- Ear, Nose, Throat
- 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 |
|---|---|---|---|
| KTI | Bronchoscope Accessory | FDA class 2 | Ear, Nose, Throat |
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