The following data is part of a premarket notification filed by Mediguide, Ltd. with the FDA for Guided Medical Positioning System Ii (gmps Ii).
Device ID | K102905 |
510k Number | K102905 |
Device Name: | GUIDED MEDICAL POSITIONING SYSTEM II (GMPS II) |
Classification | Computer, Diagnostic, Programmable |
Applicant | MEDIGUIDE, LTD. COLUMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
Contact | Jonathan S Kahan |
Correspondent | Jonathan S Kahan MEDIGUIDE, LTD. COLUMBIA SQUARE 555 THIRTEENTH STREET, NW Washington, DC 20004 -1109 |
Product Code | DQK |
CFR Regulation Number | 870.1425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-09-30 |
Decision Date | 2010-10-29 |