The following data is part of a premarket notification filed by Advanced Technology Laboratories, Inc. with the FDA for Annular Array Scanhead.
Device ID | K871856 |
510k Number | K871856 |
Device Name: | ANNULAR ARRAY SCANHEAD |
Classification | Transducer, Ultrasonic, Obstetric |
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 | HGL |
CFR Regulation Number | 884.2960 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-05-12 |
Decision Date | 1987-08-28 |