510(k) K220525

Device
RESPONDER Polysaccharide Hemostat
Applicant
Starch Medical, Inc.
510(k) number
K220525
Product code
QSY
Decision
Substantially Equivalent (SESE)
Decision date
2023-12-04
Date received
2022-02-23
Classification name
Hemostatic Wound Dressing Without Thrombin Or Other Biologics
Medical specialty
Unknown
Review panel
Unknown
Device class
U
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Alice Li
Address
2150 Ringwood Ave. San Jose CA US 95131 95131

FDA Registration Numbers

Source Documents

510(k) summary PDF

Related GUDID Devices

Primary DIBrandCompanyPublished
10899010002886Responder® Polysaccharide HemostatStarch Medical Inc.2024-06-03
00899010002834Responder® Polysaccharide HemostatStarch Medical Inc.2024-05-31

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