CONTACT LENS CASE
FDA 510(k) clearance K071081 · decided 2007-05-01
Clearance details
- K-number
- K071081
- Device name
- CONTACT LENS CASE
- Applicant
- Ningbo Kaida Rubber and Plastic Technology Co., LT
- Decision
- Substantially Equivalent
- Date received
- 2007-04-17
- Decision date
- 2007-05-01
- Days to decision
- 14 days
- Clearance type
- Traditional
- Product code
- LRX
- Device class
- 2
- Regulation number
- 886.5928
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Shanghai, CN
- Third-party review
- Yes
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.