Atlas FDA

THE TRACKER

FDA 510(k) clearance K923033 · decided 1993-06-01

Clearance details

K-number
K923033
Device name
THE TRACKER
Applicant
Epm Information Systems, Inc.
Decision
Substantially Equivalent
Date received
1992-03-23
Decision date
1993-06-01
Days to decision
435 days
Clearance type
Traditional
Product code
LXJ
Device class
2
Regulation number
890.5360
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Midlothian, VA, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VERA (K192474)Reflexion Health, Inc.2019-10-10
Vera (K182333)Reflexion Health, Inc.2019-04-09
DARI Health (K180880)Scientific Analytics, Inc.2019-03-07
Qualisys Clinical System (K171547)Qualisys AB2018-08-02
MindMotion(TM) GO (K173931)Mindmaze SA2018-05-17
UINCARE HOME (K172882)Uincare Corp.2018-05-10
MindMotionPRO (K162748)Mindmaze SA2017-04-24
Virtual Occupational Therapy Application (VOTA) (K163245)Barron Associates, Inc.2017-02-28
YuGo System (K151955)Biogaming , Ltd.2016-02-05
Vera (K150462)Reflexion Health, Inc.2015-10-30
Recovr Rehabilitation System (K151446)Recovr,Inc2015-09-18
Jintronix (K143034)Jintronix, Inc.2015-04-22

Recalls involving this device

No recalls on record reference this clearance.