The following data is part of a premarket notification filed by Dgh Technology, Inc. with the FDA for Dgh-3000a A-scan.
| Device ID | K872726 |
| 510k Number | K872726 |
| Device Name: | DGH-3000A A-SCAN |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | DGH TECHNOLOGY, INC. 446 LANCASTER AVE. Frazer, PA 19355 |
| Contact | Earl W Henderson |
| Correspondent | Earl W Henderson DGH TECHNOLOGY, INC. 446 LANCASTER AVE. Frazer, PA 19355 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-07-08 |
| Decision Date | 1987-12-04 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00857377006223 | K872726 | 000 |