510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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NASClass II

Tympanometer

21 CFR 874.1090 / Ear, Nose, Throat
FDA source (opens on fda.gov)

NAS is the FDA product code for Tympanometer, a class II device type, regulated under 21 CFR 874.1090. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
NAS
Device name
Tympanometer
Regulation
21 CFR 874.1090
Device class
Class II
Review panel
Ear, Nose, Throat
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
Yes
Ingested clearances
2
Ingested recalls
0

Clearances, product code NAS

By decision year
2 clearances under product code NAS with a decision year between 2015 and 2017, 2015 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code NAS by decision year
YearClearances
20151
20171

Applicants with the most clearances

Product code NAS
Applicants holding the most 510(k) clearances under product code NAS
ApplicantClearances
Amplivox Ltd2

Companies listing this code with FDA

Companies whose registered establishments list this code