510(k) K010559

SAUFLON MULTI LENS CARE SYSTEM by Sauflon Pharmaceuticals, Ltd. — Product Code LPN

K010559 is an FDA 510(k) premarket notification submitted by Sauflon Pharmaceuticals, Ltd. for the device "SAUFLON MULTI LENS CARE SYSTEM". The FDA issued a decision of Substantially Equivalent on December 20, 2001. The device falls under product code LPN (Accessories, Soft Lens Products), 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
December 20, 2001
Date Received
February 26, 2001
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