The following data is part of a premarket notification filed by Advanced Technology Laboratories, Inc. with the FDA for High Frequency Linear Array (hfla) Scanhead.
| Device ID | K872068 |
| 510k Number | K872068 |
| Device Name: | HIGH FREQUENCY LINEAR ARRAY (HFLA) SCANHEAD |
| Classification | Flowmeter, Blood, Cardiovascular |
| Applicant | ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
| Contact | John Dellinger |
| Correspondent | John Dellinger ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
| Product Code | DPW |
| CFR Regulation Number | 870.2100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-05-29 |
| Decision Date | 1987-09-30 |