FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE
K Number: K970247
·
Decision Mar 21, 1997
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
161
Applicant Total
529
Review Days
58
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Basic Information
- Device Name
- SMITH & NEPHEW IMAGES ARTHROSCOPE/ENT ENDOSCOPE
- K Number
- K970247
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.4760
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Smith & Nephew, Inc.
- Date Received
- January 22, 1997
- Decision Date
- March 21, 1997
- Product Code
- EOB
- 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 |
|---|---|---|---|
| EOB | Nasopharyngoscope (Flexible Or Rigid) | FDA class 2 | Ear, Nose, Throat |
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