The following data is part of a premarket notification filed by Medical Depot, Inc. with the FDA for Medical Depot-wheelchairs, Model Sentra,astaire And Viper.
| Device ID | K003783 |
| 510k Number | K003783 |
| Device Name: | MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER |
| Classification | Wheelchair, Mechanical |
| Applicant | MEDICAL DEPOT, INC. 3234 ELLA LN. New Port Richey, FL 34655 |
| Contact | Art Ward |
| Correspondent | Art Ward MEDICAL DEPOT, INC. 3234 ELLA LN. New Port Richey, FL 34655 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-07 |
| Decision Date | 2001-01-12 |