The following data is part of a premarket notification filed by Medishield, Inc. with the FDA for Hmd-2000 Battery-powered Mini-drill, The.
| Device ID | K780645 |
| 510k Number | K780645 |
| Device Name: | HMD-2000 BATTERY-POWERED MINI-DRILL, THE |
| Classification | Instrument, Surgical, Orthopedic, Dc-powered Motor And Accessory/attachment |
| Applicant | MEDISHIELD, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KIJ |
| CFR Regulation Number | 878.4820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1978-04-17 |
| Decision Date | 1978-05-03 |