The following data is part of a premarket notification filed by Pain Management Technologies with the FDA for Joint Stim, Model 1000.
| Device ID | K073386 |
| 510k Number | K073386 |
| Device Name: | JOINT STIM, MODEL 1000 |
| Classification | Stimulator, Electrical, Transcutaneous, For Arthritis |
| Applicant | PAIN MANAGEMENT TECHNOLOGIES 1340 HOME AVE. , BLDG A Akron, OH 44310 |
| Contact | Joshua Lefkovitz |
| Correspondent | Joshua Lefkovitz PAIN MANAGEMENT TECHNOLOGIES 1340 HOME AVE. , BLDG A Akron, OH 44310 |
| Product Code | NYN |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-12-03 |
| Decision Date | 2008-07-30 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08908008085147 | K073386 | 000 |