510(k) K000224

FLUROPERM 60-OK, PARAGON HDS-OK by Paragon Vision Sciences — Product Code MUW

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