The following data is part of a premarket notification filed by Medical Technologies, Inc. with the FDA for Cmap Pro.
| Device ID | K113074 |
| 510k Number | K113074 |
| Device Name: | CMAP PRO |
| Classification | Electromyograph, Diagnostic |
| Applicant | MEDICAL TECHNOLOGIES, INC. 5901-J WYOMING NE, SUITE 125 Albuquerque, NM 87106 |
| Contact | Angela Morris |
| Correspondent | Casey Conry UNDERWRITERS LABORATORIES, INC. 1285 WALT WHITMAN RD. Melville, NY 11747 |
| Product Code | IKN |
| CFR Regulation Number | 890.1375 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2011-10-17 |
| Decision Date | 2012-02-02 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CMAP PRO 85171411 4226286 Dead/Cancelled |
MED-TEK LLC 2010-11-08 |