FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
UNIVERSAL EYESHIELD
K Number: K894720
·
Decision Sep 14, 1989
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
3
Review Days
51
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Basic Information
- Device Name
- UNIVERSAL EYESHIELD
- K Number
- K894720
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4750
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Trident Medical Products, Inc.
- Date Received
- July 25, 1989
- Decision Date
- September 14, 1989
- 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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