510(k) K242228

Device
Triopsy Actuator (TMSDGB); Triopsy Biopsy Needle (BN-1825-36-01); Triopsy Biopsy Needle (BN-1825-55-01)
Applicant
Triopsy Medical, Inc.
510(k) number
K242228
Product code
KNW
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-10
Date received
2024-07-30
Regulation
876.1075
Classification name
Instrument, Biopsy
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
David Bostwick
Address
151 St. Andrews Ct. Mankato MN US 56001 56001

FDA Registration Numbers

Source Documents

510(k) summary PDF

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