The following data is part of a premarket notification filed by David Simmonds Co., Inc. with the FDA for Armboard For Intravenous Anes. In Dental.
| Device ID | K820574 |
| 510k Number | K820574 |
| Device Name: | ARMBOARD FOR INTRAVENOUS ANES. IN DENTAL |
| Classification | Table And Attachments, Operating-room |
| Applicant | DAVID SIMMONDS CO., INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | BWN |
| CFR Regulation Number | 878.4950 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1982-03-02 |
| Decision Date | 1982-03-23 |