510(k) K871714
K871714 is an FDA 510(k) premarket notification submitted by Applied Laboratories, Inc. for the device "KESTREL CONTACT LENS CASE". The FDA issued a decision of Substantially Equivalent on May 26, 1987. The device falls under product code LPN (Accessories, Soft Lens Products), a Class II device regulated under 21 CFR 886.5928. Applied Laboratories, Inc. has at least 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 26, 1987
- Date Received
- May 4, 1987
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Accessories, Soft Lens Products
- Device Class
- Class II
- Regulation Number
- 886.5928
- Review Panel
- OP
- Submission Type