FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
POST-MYDS(TM)
K Number: K930840
·
Decision Mar 1, 1994
Classifications
1
FEI Numbers
769
Registration Numbers
769
Same Product Code
54
Applicant Total
3
Review Days
377
Basic Information
- Device Name
- POST-MYDS(TM)
- K Number
- K930840
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4750
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- AUKLAND MEDICAL PLASTICS, INC.
- Date Received
- February 17, 1993
- Decision Date
- March 1, 1994
- 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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