The following data is part of a premarket notification filed by 138 Medical Supplies, Inc. with the FDA for 1818 Tens Unit.
Device ID | K992709 |
510k Number | K992709 |
Device Name: | 1818 TENS UNIT |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | 138 MEDICAL SUPPLIES, INC. 55 NORTHERN BLVD., SUITE 200 Great Neck, NY 11021 |
Contact | Susan D Goldstein-falk |
Correspondent | Susan D Goldstein-falk 138 MEDICAL SUPPLIES, INC. 55 NORTHERN BLVD., SUITE 200 Great Neck, NY 11021 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-08-11 |
Decision Date | 1999-11-09 |
Summary: | summary |