The following data is part of a premarket notification filed by American Imex with the FDA for A-tens - Model Ai-87.
Device ID | K864735 |
510k Number | K864735 |
Device Name: | A-TENS - MODEL AI-87 |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | AMERICAN IMEX 4886 PASEO DE VEGA Irvine, CA 92715 |
Contact | Joan Fong |
Correspondent | Joan Fong AMERICAN IMEX 4886 PASEO DE VEGA Irvine, CA 92715 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-04 |
Decision Date | 1987-02-20 |