FDA 510(k)
FDA class 2
Substantially Equivalent
🇬🇧 United Kingdom
POLAROID CONTACTSPOD
K Number: K131783
·
Decision Feb 21, 2014
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
81
Applicant Total
1
Review Days
249
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Basic Information
- Device Name
- POLAROID CONTACTSPOD
- K Number
- K131783
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.5928
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Viopti, Ltd.
- Date Received
- June 17, 2013
- Decision Date
- February 21, 2014
- Product Code
- LRX
- 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 |
|---|---|---|---|
| LRX | Case, Contact Lens | FDA class 2 | Ophthalmic |
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