510(k) K130734

SAUFLON MULTIPURPOSE SOLUTION by Sauflon Pharmaceuticals, Ltd. — Product Code LPN

K130734 is an FDA 510(k) premarket notification submitted by Sauflon Pharmaceuticals, Ltd. for the device "SAUFLON MULTIPURPOSE SOLUTION". The FDA issued a decision of Substantially Equivalent on May 15, 2013. 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
May 15, 2013
Date Received
March 18, 2013
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