Atlas FDA

LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM)

FDA 510(k) clearance DEN100017 · decided 2011-06-28

Clearance details

K-number
DEN100017
Device name
LIPFLOW THERMAL PULSATION SYSTEM (FORMERLY MANUAL MINI SYSTEM)
Applicant
Tearscience, Inc.
Decision
Unknown
Date received
2010-08-09
Decision date
2011-06-28
Days to decision
323 days
Clearance type
Post-NSE
Product code
ORZ
Device class
2
Regulation number
886.5200
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Morrisville, NC, US
Third-party review
No
Expedited review
No

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iLux Instrument, iLux Disposable (K172645)Tear Film Innovations, Inc.2017-12-26
LipiFlow Thermal Pulsation System (K161357)Tearscience, Inc.2016-11-04
LIPIFLOW THERMAL PULSATION SYSTEM (K133127)Tearscience, Inc.2013-12-23
LIPIFLOW THERMAL PULSATION SYSTEM (K112704)Tearscience, Inc.2011-12-19

Recalls involving this device

No recalls on record reference this clearance.