The following data is part of a premarket notification filed by Metron Medical Australia Pty Ltd with the FDA for Sonic, Model So-100.
Device ID | K000593 |
510k Number | K000593 |
Device Name: | SONIC, MODEL SO-100 |
Classification | Ultrasonic Diathermy For Use In Applying Therapeutic Deep Heat |
Applicant | METRON MEDICAL AUSTRALIA PTY LTD 57 ASTER AVE. Carrum Downs, Victoria, AU 3201 |
Contact | Rob Hopkins |
Correspondent | Rob Hopkins METRON MEDICAL AUSTRALIA PTY LTD 57 ASTER AVE. Carrum Downs, Victoria, AU 3201 |
Product Code | IMI |
CFR Regulation Number | 890.5300 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2000-02-22 |
Decision Date | 2000-08-04 |