510(k) K790878
K790878 is an FDA 510(k) premarket notification submitted by Vicon Instrument Co. for the device "SCREENING AUDIOMETER, HIGH FREQUENCY". The FDA issued a decision of Substantially Equivalent on August 3, 1979. The device falls under product code EWO (Audiometer), a Class II device regulated under 21 CFR 874.1050. Vicon Instrument Co. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 3, 1979
- Date Received
- May 7, 1979
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Audiometer
- Device Class
- Class II
- Regulation Number
- 874.1050
- Review Panel
- EN
- Submission Type