The following data is part of a premarket notification filed by Medical Research Laboratories, Inc. with the FDA for Modified Mrl Neuroprobe System V.
Device ID | K884869 |
510k Number | K884869 |
Device Name: | MODIFIED MRL NEUROPROBE SYSTEM V |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | MEDICAL RESEARCH LABORATORIES, INC. 6457 W. HOWARD ST. Niles, IL 60648 |
Contact | Dilip Mehta |
Correspondent | Dilip Mehta MEDICAL RESEARCH LABORATORIES, INC. 6457 W. HOWARD ST. Niles, IL 60648 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-11-21 |
Decision Date | 1989-06-06 |