The following data is part of a premarket notification filed by Amsco Co. with the FDA for Table, Examining-two Eighty.
| Device ID | K782064 |
| 510k Number | K782064 |
| Device Name: | TABLE, EXAMINING-TWO EIGHTY |
| Classification | Unit, Examining/treatment, Ent |
| Applicant | AMSCO CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | ETF |
| CFR Regulation Number | 874.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-12-13 |
| Decision Date | 1978-12-28 |