FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT
K Number: K925173
·
Decision Jan 15, 1993
Classifications
1
FEI Numbers
110
Registration Numbers
110
Same Product Code
45
Applicant Total
9
Review Days
93
Basic Information
- Device Name
- BOOMERANG TURBINATE GLOVE AND SEPTAL SPLINT
- K Number
- K925173
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.4780
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- WESTMED INTL.
- Date Received
- October 14, 1992
- Decision Date
- January 15, 1993
- Product Code
- LYA
- 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 |
|---|---|---|---|
| LYA | Splint, Intranasal Septal | FDA class 1 | Ear, Nose, Throat |
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