510(k) K052809

SAUFLON FLAT COLOURED LENS CASE by Sauflon Pharmaceuticals, Ltd. — Product Code LRX

K052809 is an FDA 510(k) premarket notification submitted by Sauflon Pharmaceuticals, Ltd. for the device "SAUFLON FLAT COLOURED LENS CASE". The FDA issued a decision of Substantially Equivalent on November 2, 2005. The device falls under product code LRX (Case, Contact Lens), a Class II device regulated under 21 CFR 886.5928. Sauflon Pharmaceuticals, Ltd. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 2, 2005
Date Received
October 4, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Case, Contact Lens
Device Class
Class II
Regulation Number
886.5928
Review Panel
OP
Submission Type