The following data is part of a premarket notification filed by American Hospital Supply Corp. with the FDA for Container W/priming Solution.
| Device ID | K830343 |
| 510k Number | K830343 |
| Device Name: | CONTAINER W/PRIMING SOLUTION |
| Classification | Regulator, Vacuum |
| Applicant | AMERICAN HOSPITAL SUPPLY CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KDP |
| CFR Regulation Number | 880.6740 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-02-01 |
| Decision Date | 1983-03-17 |