The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Dimensionall Rotator.
| Device ID | K790753 |
| 510k Number | K790753 |
| Device Name: | DIMENSIONALL ROTATOR |
| Classification | Shaker/stirrer |
| Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JRQ |
| CFR Regulation Number | 862.2050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-04-17 |
| Decision Date | 1979-06-28 |