FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TAPELESS EYE SHIELD
K Number: K872659
·
Decision Jul 27, 1987
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
2
Review Days
20
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Basic Information
- Device Name
- TAPELESS EYE SHIELD
- K Number
- K872659
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4750
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Precision Therapeutics, Inc.
- Date Received
- July 7, 1987
- Decision Date
- July 27, 1987
- Product Code
- HOY
- 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 |
|---|---|---|---|
| HOY | Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear) | FDA class 1 | Ophthalmic |
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Other Clearances by Precision Therapeutics, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K864810 | LIDSPLINT | Jan 20, 1987 | Substantially Equivalent |