FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
GOGGLE SAFEGUARD
K Number: K931254
·
Decision Nov 12, 1993
Classifications
1
FEI Numbers
712
Registration Numbers
712
Same Product Code
54
Applicant Total
2
Review Days
245
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Basic Information
- Device Name
- GOGGLE SAFEGUARD
- K Number
- K931254
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4750
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Sellstrom Mfg. Co.
- Date Received
- March 12, 1993
- Decision Date
- November 12, 1993
- 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 Sellstrom Mfg. Co.
| K Number | Device Name | ||
|---|---|---|---|
| K944857 | GOGGLE SAFEGUARD | Dec 15, 1994 | Substantially Equivalent |