The following data is part of a premarket notification filed by Parker Treadmill Co., Inc. with the FDA for Parker Model Pe.
| Device ID | K950377 |
| 510k Number | K950377 |
| Device Name: | PARKER MODEL PE |
| Classification | Treadmill, Powered |
| Applicant | PARKER TREADMILL CO., INC. 368 INDUSTRY DR. Auburn, AL 36830 |
| Contact | Robert Parker |
| Correspondent | Robert Parker PARKER TREADMILL CO., INC. 368 INDUSTRY DR. Auburn, AL 36830 |
| Product Code | IOL |
| CFR Regulation Number | 890.5380 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-01-31 |
| Decision Date | 1995-09-06 |