The following data is part of a premarket notification filed by Vismed, Inc. with the FDA for Ld 400.
| Device ID | K930937 |
| 510k Number | K930937 |
| Device Name: | LD 400 |
| Classification | Perimeter, Automatic, Ac-powered |
| Applicant | VISMED, INC. 10373 ROSELLE ST., SUITE 4 San Diego, CA 92121 |
| Contact | Rich Eberhardt |
| Correspondent | Rich Eberhardt VISMED, INC. 10373 ROSELLE ST., SUITE 4 San Diego, CA 92121 |
| Product Code | HPT |
| CFR Regulation Number | 886.1605 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-23 |
| Decision Date | 1993-10-18 |