510(k) DEN100017

LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM) by Tearscience, Inc. — Product Code ORZ

DEN100017 is an FDA 510(k) premarket notification submitted by Tearscience, Inc. for the device "LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM)". The FDA issued a decision of De Novo Granted on June 28, 2011. The device falls under product code ORZ (Eyelid Thermal Pulsation System), a Class II device regulated under 21 CFR 886.5200. Tearscience, Inc. has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
DENG (De Novo Granted)
Decision Date
June 28, 2011
Date Received
August 9, 2010
Clearance Type
Post-NSE
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Eyelid Thermal Pulsation System
Device Class
Class II
Regulation Number
886.5200
Review Panel
OP
Submission Type

Therapeutic application of heat and massage to the eyelids.