510(k) K000224
K000224 is an FDA 510(k) premarket notification submitted by Paragon Vision Sciences for the device "FLUROPERM 60-OK, PARAGON HDS-OK". The FDA issued a decision of SESU on April 17, 2000. The device falls under product code MUW (Lens, Contact (Orthokeratology)), a Class II device regulated under 21 CFR 886.5916. Paragon Vision Sciences has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESU ()
- Decision Date
- April 17, 2000
- Date Received
- January 24, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lens, Contact (Orthokeratology)
- Device Class
- Class II
- Regulation Number
- 886.5916
- Review Panel
- OP
- Submission Type