BILIARY INDWELLING STENT

Stents, Drains And Dilators For The Biliary Ducts

HOBBS MEDICAL, INC.

The following data is part of a premarket notification filed by Hobbs Medical, Inc. with the FDA for Biliary Indwelling Stent.

Pre-market Notification Details

Device IDK834351
510k NumberK834351
Device Name:BILIARY INDWELLING STENT
ClassificationStents, Drains And Dilators For The Biliary Ducts
Applicant HOBBS MEDICAL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeFGE  
CFR Regulation Number876.5010 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-12-13
Decision Date1984-03-22

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
M84960050 K834351 000
M84965050 K834351 000
M84965060 K834351 000
M84965070 K834351 000
M84965080 K834351 000
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M84961060 K834351 000
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M84965270 K834351 000
M84965280 K834351 000
M84965290 K834351 000
M84965300 K834351 000
M84965310 K834351 000
M84961090 K834351 000

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