510(k) K942722

MODULE PROGRAM by Electone, Inc. — Product Code LRB

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