FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
RELIEF VALVE-HONAN INTRAOC. PRESSURE
K Number: K820526
·
Decision Mar 25, 1982
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
5
Applicant Total
3
Review Days
27
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Basic Information
- Device Name
- RELIEF VALVE-HONAN INTRAOC. PRESSURE
- K Number
- K820526
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.4610
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- The Lebanon Corp.
- Date Received
- February 26, 1982
- Decision Date
- March 25, 1982
- Product Code
- LCC
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| LCC | Applicator, Ocular Pressure | FDA class 2 | Ophthalmic |
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