HSW GMBH ARTHROSCOPE

Arthroscope

HENKE SASS WOLF OF AMERICA, INC.

The following data is part of a premarket notification filed by Henke Sass Wolf Of America, Inc. with the FDA for Hsw Gmbh Arthroscope.

Pre-market Notification Details

Device IDK962075
510k NumberK962075
Device Name:HSW GMBH ARTHROSCOPE
ClassificationArthroscope
Applicant HENKE SASS WOLF OF AMERICA, INC. SOROCO INDUSTRIAL PARK ROUTE 131 Southbridge,  MA  01550
ContactJohn M Smith
CorrespondentJohn M Smith
HENKE SASS WOLF OF AMERICA, INC. SOROCO INDUSTRIAL PARK ROUTE 131 Southbridge,  MA  01550
Product CodeHRX  
CFR Regulation Number888.1100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1996-05-28
Decision Date1997-01-17

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20845854044206 K962075 000
30845854031821 K962075 000
30845854031838 K962075 000
30845854031845 K962075 000
30845854031852 K962075 000
30845854031869 K962075 000
30845854031876 K962075 000
30845854031883 K962075 000
30845854031890 K962075 000
30845854031814 K962075 000
30845854031791 K962075 000
30845854012851 K962075 000
30845854012998 K962075 000
30845854013131 K962075 000
30845854027107 K962075 000
30845854027114 K962075 000
30845854028821 K962075 000
30845854031777 K962075 000
30845854031784 K962075 000
30845854031906 K962075 000
30845854031913 K962075 000
30845854031920 K962075 000
30845854040441 K962075 000
30845854040502 K962075 000
30845854040557 K962075 000
30845854040564 K962075 000
30845854080577 K962075 000
30845854605749 K962075 000
30845854605756 K962075 000
30845854605763 K962075 000
30845854036413 K962075 000
30845854036406 K962075 000
30845854032026 K962075 000
30845854032064 K962075 000
30845854032705 K962075 000
30845854035973 K962075 000
30845854035980 K962075 000
30845854035997 K962075 000
30845854036000 K962075 000
30845854036017 K962075 000
30845854605770 K962075 000

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