The following data is part of a premarket notification filed by Biomedical Life Systems, Inc. with the FDA for Electro-nerve Stimulator Tens Model Systems 2000/a.
Device ID | K905377 |
510k Number | K905377 |
Device Name: | ELECTRO-NERVE STIMULATOR TENS MODEL SYSTEMS 2000/A |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | BIOMEDICAL LIFE SYSTEMS, INC. 1285 STONE DR. #103 P.O. BOX 128 San Marcos, CA 92069 |
Contact | Richard G Saxon |
Correspondent | Richard G Saxon BIOMEDICAL LIFE SYSTEMS, INC. 1285 STONE DR. #103 P.O. BOX 128 San Marcos, CA 92069 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-11-30 |
Decision Date | 1991-06-04 |