510(k) K760166
K760166 is an FDA 510(k) premarket notification submitted by Farrall Instruments, Inc. for the device "STIMULATOR, SONIC CONTROL (AS-1)". The FDA issued a decision of Substantially Equivalent on July 20, 1976. The device falls under product code HCB (Device, Aversive Conditioning), a Class II device regulated under 21 CFR 882.5235. Farrall Instruments, Inc. has at least 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1976
- Date Received
- July 6, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Aversive Conditioning
- Device Class
- Class II
- Regulation Number
- 882.5235
- Review Panel
- NE
- Submission Type