FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
ANTRUM & ATTIC MIRROR
K Number: K833601
·
Decision Jan 3, 1984
Classifications
1
FEI Numbers
106
Registration Numbers
106
Same Product Code
8
Applicant Total
24
Review Days
83
Basic Information
- Device Name
- ANTRUM & ATTIC MIRROR
- K Number
- K833601
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 874.4420
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Applicant
- MICROTEK MEDICAL, INC.
- Date Received
- October 12, 1983
- Decision Date
- January 3, 1984
- Product Code
- KAI
- 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 |
|---|---|---|---|
| KAI | Mirror, Ent | FDA class 1 | Ear, Nose, Throat |
Similar 510(k) Clearances
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