The following data is part of a premarket notification filed by Jedmed Instrument Co. with the FDA for Mobile Treatment Cart.
| Device ID | K910243 |
| 510k Number | K910243 |
| Device Name: | MOBILE TREATMENT CART |
| Classification | Unit, Examining/treatment, Ent |
| Applicant | JEDMED INSTRUMENT CO. 6096 LEMAY FERRY RD. St.louis, MO 63129 -2217 |
| Contact | Craig Rapp |
| Correspondent | Craig Rapp JEDMED INSTRUMENT CO. 6096 LEMAY FERRY RD. St.louis, MO 63129 -2217 |
| Product Code | ETF |
| CFR Regulation Number | 874.5300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1991-01-22 |
| Decision Date | 1991-04-17 |