Atlas FDA

XSTAT

FDA 510(k) clearance DEN130016 · decided 2014-04-03

Clearance details

K-number
DEN130016
Device name
XSTAT
Applicant
Revmedx, Inc.
Decision
Unknown
Date received
2013-01-30
Decision date
2014-04-03
Days to decision
428 days
Clearance type
Direct
Product code
PGZ
Device class
2
Regulation number
878.4452
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Washington, DC, 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
XSTAT P15 (K253290)Revmedx, Inc.2025-11-12
XSTAT 30 Pouch (K210676)Revmedx, Inc.2021-08-27
XSTAT 30, 1-Pack (K180051)Revmedx, Inc.2018-05-18
XSTAT 30, 3-Pack; XSTAT 30, 1-Pack; XSTAT 12, 3 Pack; XSTAT 12, 1 Pack (K170334)Revmedx, Inc.2017-05-01
XSTAT-12, 3-Pack, XSTAT-12, 1-Pack (K161020)Revmedx, Inc.2016-07-28
XSTAT 30, 3-PACK, XSTAT 30, 1-PACK (K152624)Revmedx, Inc.2015-12-07

Recalls involving this device

No recalls on record reference this clearance.