The following data is part of a premarket notification filed by Barnes,richardson & Colburn with the FDA for V-1504 Vertical Platform Lift.
| Device ID | K960739 |
| 510k Number | K960739 |
| Device Name: | V-1504 VERTICAL PLATFORM LIFT |
| Classification | Elevator, Wheelchair, Portable |
| Applicant | BARNES,RICHARDSON & COLBURN 1225 EYE STREET, N.W. Washington, DC 20005 |
| Contact | Ansis M Helmanis |
| Correspondent | Ansis M Helmanis BARNES,RICHARDSON & COLBURN 1225 EYE STREET, N.W. Washington, DC 20005 |
| Product Code | ING |
| CFR Regulation Number | 890.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1996-02-23 |
| Decision Date | 1996-04-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10688503410006 | K960739 | 000 |
| 10688503230000 | K960739 | 000 |
| 10688503210002 | K960739 | 000 |