510(k) K090611

Device
REVOLUTION FULL CORE BIOPSY
Applicant
Inrad
510(k) number
K090611
Product code
KNW
Decision
Substantially Equivalent (SESE)
Decision date
2009-06-04
Date received
2009-03-06
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
No

Related Records

Applicant Contact

Contact
MELISSA LALOMIA
Address
4375 Donker Ct. SE Kentwood MI US 49512 49512

FDA Registration Numbers

Source Documents

510(k) summary PDF

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