The following data is part of a premarket notification filed by D.t. Davis Enterprises Ltd. with the FDA for Hoverjack Air Patient Lift Device.
| Device ID | K041503 |
| 510k Number | K041503 |
| Device Name: | HOVERJACK AIR PATIENT LIFT DEVICE |
| Classification | Lift, Patient, Ac-powered |
| Applicant | D.T. DAVIS ENTERPRISES LTD. 513 S. CLEWELL ST. Bethlehem, PA 18015 -4537 |
| Contact | David T Davis |
| Correspondent | David T Davis D.T. DAVIS ENTERPRISES LTD. 513 S. CLEWELL ST. Bethlehem, PA 18015 -4537 |
| Product Code | FNG |
| CFR Regulation Number | 880.5500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-07 |
| Decision Date | 2004-08-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816299010435 | K041503 | 000 |
| 00816299010428 | K041503 | 000 |
| 00816299010411 | K041503 | 000 |
| 00816299010404 | K041503 | 000 |