The following data is part of a premarket notification filed by U.s. Table, Inc. with the FDA for Ptt 6200 Elevation Therapy Table.
| Device ID | K953622 |
| 510k Number | K953622 |
| Device Name: | PTT 6200 ELEVATION THERAPY TABLE |
| Classification | Table, Powered |
| Applicant | U.S. TABLE, INC. 11233 WASHINGTON HIGHWAY Glen Allen, VA 23059 |
| Contact | Brenda Cassell |
| Correspondent | Brenda Cassell U.S. TABLE, INC. 11233 WASHINGTON HIGHWAY Glen Allen, VA 23059 |
| Product Code | INQ |
| CFR Regulation Number | 890.3760 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-08-03 |
| Decision Date | 1995-09-11 |