The following data is part of a premarket notification filed by American Sterilizer Co. with the FDA for Amsco Endoscopy Table.
| Device ID | K821749 |
| 510k Number | K821749 |
| Device Name: | AMSCO ENDOSCOPY TABLE |
| Classification | Table, Operating-room, Electrical |
| Applicant | AMERICAN STERILIZER CO. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GDC |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-06-15 |
| Decision Date | 1982-07-09 |