The following data is part of a premarket notification filed by Advanced Technology Laboratories, Inc. with the FDA for Atl's Ultramark 6 Ultrasound System.
Device ID | K864657 |
510k Number | K864657 |
Device Name: | ATL'S ULTRAMARK 6 ULTRASOUND SYSTEM |
Classification | Echocardiograph |
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 | DXK |
CFR Regulation Number | 870.2330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-11-28 |
Decision Date | 1987-02-02 |