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510(k) K851780

Device
25-230 TO 25-390 VARIOUS NEEDLE HOLDERS
Applicant
ARTIBERIA
510(k) number
K851780
Product code
FHQ  
Decision
Substantially Equivalent (SESE)
Decision date
1985-06-20
Date received
1985-04-25
Regulation
876.4730
Classification name
Holder, Needle, Gastroenterologic
Medical specialty
Gastroenterology/Urology
Review panel
Gastroenterology/Urology
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
GIL M SANCHEZ
Address
4518 Los Ranchitos San Antonio TX US 78233 78233

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code FHQ  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K974327WINGED NEEDLE HOLDERPhx Technologies Corp.1998-01-09
K924196LAPAROSCOPIC NEEDLE HOLDERNusurg, Inc.1993-06-25
K930330ENDOSCOPIC NEEDLEHOLDER, MODIFICATIONHolmed Corp.1993-06-08
K920706MAGNETIC POINT GUARD FOR SURGICAL NEEDLESRetrax1993-05-26
K85177925-100,25-220 VARIOUS NEEDLE HOLDERSArtiberia1985-06-20
K771859NEEDLE HOLDER, MICROVASCULAREdward Weck, Inc.1977-10-04

Legacy Summary#

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FDA Review#

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