The following data is part of a premarket notification filed by Ausonics Pty Ltd. with the FDA for Wwds-005 Human Rectal Probe.
| Device ID | K883079 |
| 510k Number | K883079 |
| Device Name: | WWDS-005 HUMAN RECTAL PROBE |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | AUSONICS PTY LTD. 40 CRANE HILL RD. Suffield, CT 06078 |
| Contact | C Nealon |
| Correspondent | C Nealon AUSONICS PTY LTD. 40 CRANE HILL RD. Suffield, CT 06078 |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1988-07-21 |
| Decision Date | 1988-12-14 |