510(k) K942722
K942722 is an FDA 510(k) premarket notification submitted by Electone, Inc. for the device "MODULE PROGRAM". The FDA issued a decision of Substantially Equivalent on September 6, 1994. The device falls under product code LRB (Face Plate Hearing Aid), a Class I device regulated under 21 CFR 874.3300. Electone, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 6, 1994
- Date Received
- June 9, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Face Plate Hearing Aid
- Device Class
- Class I
- Regulation Number
- 874.3300
- Review Panel
- EN
- Submission Type