510(k) K212423

Device
EndoDrill® Model X
Applicant
Bibbinstruments AB
510(k) number
K212423
Product code
FCG
Decision
Substantially Equivalent (SESE)
Decision date
2023-03-29
Date received
2021-08-04
Regulation
876.1075
Classification name
Biopsy Needle
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Marie Grey
Address
Scheelevagen 2 Lund SE S-223 63 S-223 63

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code FCG#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K191472Biopsy NeedleUshare Medical, Inc.2020-01-29
K181756Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial NeedleApriomed AB2018-12-18
K180668Single Use Aspiration Needle NA-U401SX-4025/NA-U401SX-4025NOlympus Medical Systems Corp.2018-11-15
K180363Clear-Tip EUS-FNAFinemedix Co., Ltd.2018-11-01
K181994Single Use Aspiration Needle NA-U201HOlympus Medical Systems Corp.2018-10-31
K180449Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp.2018-06-08