FMS DUO

Arthroscope

FUTURE MEDICAL SYSTEMS, INC.

The following data is part of a premarket notification filed by Future Medical Systems, Inc. with the FDA for Fms Duo.

Pre-market Notification Details

Device IDK954465
510k NumberK954465
Device Name:FMS DUO
ClassificationArthroscope
Applicant FUTURE MEDICAL SYSTEMS, INC. 205 EAST 63RD ST. SUITE 7A New York City,  NY  10021
ContactPatrick Janin
CorrespondentPatrick Janin
FUTURE MEDICAL SYSTEMS, INC. 205 EAST 63RD ST. SUITE 7A New York City,  NY  10021
Product CodeHRX  
CFR Regulation Number888.1100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-09-25
Decision Date1995-11-09

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
20886705015853 K954465 000
20886705000354 K954465 000
20886705000385 K954465 000
20886705000392 K954465 000
20886705000460 K954465 000
20886705000477 K954465 000
20886705000514 K954465 000
20886705000576 K954465 000
20886705000590 K954465 000
20886705000613 K954465 000
20886705000675 K954465 000
20886705000736 K954465 000
20886705000750 K954465 000
10886705017089 K954465 000
10886705016440 K954465 000
10886705017010 K954465 000
10886705017249 K954465 000
10886705017256 K954465 000
20886705000330 K954465 000

Trademark Results [FMS DUO]

Mark Image

Registration | Serial
Company
Trademark
Application Date
FMS DUO
FMS DUO
74673544 2066192 Live/Registered
FMS Future Medical System S.A.
1995-05-15

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