510(k) K234131

Device
Resolv Endoscopic Hemostat System
Applicant
Hemostasis, LLC
510(k) number
K234131
Product code
QAU
Decision
Substantially Equivalent (SESE)
Decision date
2024-07-26
Date received
2023-12-28
Regulation
878.4456
Classification name
Hemostatic Device For Endoscopic Gastrointestinal Use
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Lakshmi Ganesh Bollina
Address
5000 Township Pkwy. St. Paul MN US 55110 55110

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QAU#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253924PuraStat3-D Matrix Europe SAS2026-01-07
K240994NexpowderNextbiomedical Co., Ltd.2024-11-27
K242250PuraStat3-D Matrix Europe SAS2024-10-22
K222481PuraStat3-D Matrix, Inc.2023-02-28
K202929NexpowderNextbiomedical Co., Ltd.2022-09-16
K210098PuraStat-GI3-D Matrix, Inc.2021-06-25
K190677EndoClotEndoclot Plus Co., Ltd.2021-01-29
K200972Hemospray Endoscopic HemostatWilson-Cook Medical, Inc.2020-06-10
DEN170015Hemospray Endoscopic HemostatWilson-Cook Medical, Inc.2018-05-07