The following data is part of a premarket notification filed by Regional Master Corp. with the FDA for Nerve Finder.
Device ID | K853477 |
510k Number | K853477 |
Device Name: | NERVE FINDER |
Classification | Stimulator, Nerve, Battery-powered |
Applicant | REGIONAL MASTER CORP. P.O. BOX 431832 Miami, FL 33143 |
Contact | Margarita Plaza |
Correspondent | Margarita Plaza REGIONAL MASTER CORP. P.O. BOX 431832 Miami, FL 33143 |
Product Code | BXN |
CFR Regulation Number | 868.2775 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-08-14 |
Decision Date | 1986-01-14 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NERVE FINDER 73375953 1273180 Dead/Cancelled |
Regional Master Corporation 1982-07-22 |
![]() NERVE FINDER 72113820 0732783 Dead/Cancelled |
ELECTRONIC AIDS, INC. 1961-02-16 |