The following data is part of a premarket notification filed by Future Medical Systems, Inc. with the FDA for Fms Duo.
| Device ID | K954465 |
| 510k Number | K954465 |
| Device Name: | FMS DUO |
| Classification | Arthroscope |
| Applicant | FUTURE MEDICAL SYSTEMS, INC. 205 EAST 63RD ST. SUITE 7A New York City, NY 10021 |
| Contact | Patrick Janin |
| Correspondent | Patrick Janin FUTURE MEDICAL SYSTEMS, INC. 205 EAST 63RD ST. SUITE 7A New York City, NY 10021 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-09-25 |
| Decision Date | 1995-11-09 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 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 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FMS DUO 74673544 2066192 Live/Registered |
FMS Future Medical System S.A. 1995-05-15 |