The following data is part of a premarket notification filed by Biomedical Life Systems, Inc. with the FDA for Electro-nerve Stimulator Tens Model B5/skn.
Device ID | K871125 |
510k Number | K871125 |
Device Name: | ELECTRO-NERVE STIMULATOR TENS MODEL B5/SKN |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | BIOMEDICAL LIFE SYSTEMS, INC. P.O. BOX 39636 Los Angeles, CA 90039 |
Contact | Richard G Saxon |
Correspondent | Richard G Saxon BIOMEDICAL LIFE SYSTEMS, INC. P.O. BOX 39636 Los Angeles, CA 90039 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-03-20 |
Decision Date | 1987-06-02 |