PUNCTURENEEDLE

Instrument, Biopsy

FERGUSON MEDICAL

The following data is part of a premarket notification filed by Ferguson Medical with the FDA for Punctureneedle.

Pre-market Notification Details

Device IDK963794
510k NumberK963794
Device Name:PUNCTURENEEDLE
ClassificationInstrument, Biopsy
Applicant FERGUSON MEDICAL 3407 BAY AVE. Chico,  CA  95973 -8619
ContactFrank Ferguson
CorrespondentFrank Ferguson
FERGUSON MEDICAL 3407 BAY AVE. Chico,  CA  95973 -8619
Product CodeKNW  
CFR Regulation Number876.1075 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-09-20
Decision Date1998-03-19
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00884838073470 K963794 000
00884838072749 K963794 000
00884838072732 K963794 000
00884838072725 K963794 000
00884838072718 K963794 000
00884838072701 K963794 000
00884838072695 K963794 000
00884838072688 K963794 000
00884838072671 K963794 000
00884838072626 K963794 000
00884838072824 K963794 000
00884838072831 K963794 000
00884838072848 K963794 000
00884838073302 K963794 000
00884838073296 K963794 000
00884838072916 K963794 000
00884838072909 K963794 000
00884838072893 K963794 000
00884838072886 K963794 000
00884838072879 K963794 000
00884838072862 K963794 000
00884838072855 K963794 000
00884838072619 K963794 000

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.