Atlas FDA

Hemospray Endoscopic Hemostat

FDA 510(k) clearance K200972 · decided 2020-06-10

Clearance details

K-number
K200972
Device name
Hemospray Endoscopic Hemostat
Applicant
Wilson-Cook Medical, Inc.
Decision
Substantially Equivalent
Date received
2020-04-13
Decision date
2020-06-10
Days to decision
58 days
Clearance type
Traditional
Product code
QAU
Device class
2
Regulation number
878.4456
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Winston-Salem, NC, 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
PuraStat GI (K261503)3-D Matrix, Inc.2026-08-03
Hemospray Endoscopic Hemostat (HEMO-[X]) (K253302)Wilson-Cook Medical, Inc.2026-06-02
PuraStat (K253924)3-D Matrix Europe SAS2026-01-07
Nexpowder (K240994)Nextbiomedical Co., Ltd.2024-11-27
PuraStat (K242250)3-D Matrix Europe SAS2024-10-22
Resolv Endoscopic Hemostat System (K234131)Hemostasis, LLC2024-07-26
PuraStat (K222481)3-D Matrix, Inc.2023-02-28
Nexpowder (K202929)Nextbiomedical Co., Ltd.2022-09-16
PuraStat-GI (K210098)3-D Matrix, Inc.2021-06-25
EndoClot (K190677)Endoclot Plus Co., Ltd.2021-01-29
Hemospray Endoscopic Hemostat (DEN170015)Wilson-Cook Medical, Inc.2018-05-07

Recalls involving this device

RecordFirmDate
Cook Medical Hemo-7 Hemospray Endoscopic Hemostat, REF G56572, 2.8 mm, Sterile; and Hemo-1 recall (Z-0036-2025)Wilson-Cook Medical Inc.2024-10-16
Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-7, REF G56572; b) HEMO-7-EU recall (Z-1978-2023)Wilson-Cook Medical Inc.2023-06-21
Hemospray Endoscopic Hemostat: Reference Part Numbers: a) HEMO-10, REF G21049; b) HEMO-10- recall (Z-1979-2023)Wilson-Cook Medical Inc.2023-06-21