The following data is part of a premarket notification filed by Diasonics, Inc. with the FDA for Diasonics Spa 5.o 27mm Probe.
Device ID | K864758 |
510k Number | K864758 |
Device Name: | DIASONICS SPA 5.O 27MM PROBE |
Classification | Transducer, Ultrasonic, Diagnostic |
Applicant | DIASONICS, INC. 1565 BARBER LN. Milipitas, CA 95035 |
Contact | Gary M Agatep |
Correspondent | Gary M Agatep DIASONICS, INC. 1565 BARBER LN. Milipitas, CA 95035 |
Product Code | ITX |
CFR Regulation Number | 892.1570 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1986-12-05 |
Decision Date | 1987-03-10 |