The following data is part of a premarket notification filed by Amplifon S.p.a. with the FDA for Amplaid A724 And A728.
Device ID | K992370 |
510k Number | K992370 |
Device Name: | AMPLAID A724 AND A728 |
Classification | Tester, Auditory Impedance |
Applicant | AMPLIFON S.P.A. P.O. BOX 7007 Deerfield, IL 60015 |
Contact | Daniel Kamm |
Correspondent | Daniel Kamm AMPLIFON S.P.A. P.O. BOX 7007 Deerfield, IL 60015 |
Product Code | ETY |
CFR Regulation Number | 874.1090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1999-07-15 |
Decision Date | 1999-09-20 |
Summary: | summary |