The following data is part of a premarket notification filed by Far Orthopedics, Inc. with the FDA for Metricom.
Device ID | K860225 |
510k Number | K860225 |
Device Name: | METRICOM |
Classification | Device, Sensing, Optical Contour |
Applicant | FAR ORTHOPEDICS, INC. 2875 SABOURIN MONTREAL - QUE - H4S 1M9 Canada, CA |
Contact | Raab, Ph.d. |
Correspondent | Raab, Ph.d. FAR ORTHOPEDICS, INC. 2875 SABOURIN MONTREAL - QUE - H4S 1M9 Canada, CA |
Product Code | LDK |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-01-22 |
Decision Date | 1986-02-11 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
METRICOM 75144414 2210004 Dead/Cancelled |
CIVITAS WIRELESS SOLUTIONS, LLC 1996-08-05 |
METRICOM 75144413 2089160 Dead/Cancelled |
CIVITAS WIRELESS SOLUTIONS, LLC 1996-08-05 |
METRICOM 73779373 1613592 Dead/Cancelled |
METRICOM, INC. 1989-02-06 |
METRICOM 73779322 1604403 Dead/Cancelled |
METRICOM, INC. 1989-02-06 |