The following data is part of a premarket notification filed by Ausonics Pty Ltd. with the FDA for Alpha S/d Diagnostic X-ray Mammography Unit.
Device ID | K863710 |
510k Number | K863710 |
Device Name: | ALPHA S/D DIAGNOSTIC X-RAY MAMMOGRAPHY UNIT |
Classification | System, X-ray, Mammographic |
Applicant | AUSONICS PTY LTD. 40 CRANE HILL RD. Suffield, CT 06078 |
Contact | William C Nealon |
Correspondent | William C Nealon AUSONICS PTY LTD. 40 CRANE HILL RD. Suffield, CT 06078 |
Product Code | IZH |
CFR Regulation Number | 892.1710 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-09-23 |
Decision Date | 1986-10-14 |