The following data is part of a premarket notification filed by Jetco Of America with the FDA for Electronic Pain Relievers.
| Device ID | K883811 |
| 510k Number | K883811 |
| Device Name: | ELECTRONIC PAIN RELIEVERS |
| Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
| Applicant | JETCO OF AMERICA 3003 WEST NORTHERN AVE., STE. 5 Phoenix, AZ 85051 |
| Contact | L Johari |
| Correspondent | L Johari JETCO OF AMERICA 3003 WEST NORTHERN AVE., STE. 5 Phoenix, AZ 85051 |
| Product Code | GZJ |
| CFR Regulation Number | 882.5890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-09-08 |
| Decision Date | 1989-10-24 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08908008085161 | K883811 | 000 |