The following data is part of a premarket notification filed by Advanced Technology Laboratories, Inc. with the FDA for Ultrasonic Pulsed Doppler Imaging System.
Device ID | K903348 |
510k Number | K903348 |
Device Name: | ULTRASONIC PULSED DOPPLER IMAGING SYSTEM |
Classification | Transducer, Ultrasonic, Obstetric |
Applicant | ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
Contact | Terrence J Sweeney |
Correspondent | Terrence J Sweeney ADVANCED TECHNOLOGY LABORATORIES, INC. 22100 BOTHELL EVERETT HWY. P.O. BOX 3003 Bothell, WA 98041 -3003 |
Product Code | HGL |
CFR Regulation Number | 884.2960 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-07-26 |
Decision Date | 1990-10-22 |