The following data is part of a premarket notification filed by Futuremed Div. Of Future Impex Corp. with the FDA for Tens Device For Relief Of Chronic Pain.
Device ID | K864114 |
510k Number | K864114 |
Device Name: | TENS DEVICE FOR RELIEF OF CHRONIC PAIN |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | FUTUREMED DIV. OF FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deer Park, NY 11729 |
Contact | Morad Davoudzadeh |
Correspondent | Morad Davoudzadeh FUTUREMED DIV. OF FUTURE IMPEX CORP. 2076 DEER PARK AVE. Deer Park, NY 11729 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-10-21 |
Decision Date | 1987-04-01 |