510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K891988Substantially Equivalent

Amplaid A308 Clinical Audiometer

Amplus Corp., Boulder CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K891988 is the FDA 510(k) clearance record for AMPLAID A308 CLINICAL AUDIOMETER, a class II device, cleared for Amplus Corp. on under FDA product code EWO (Audiometer). FDA records list 4 510(k) clearances for Amplus Corp., from to . As of , FDA records show no recalls naming K891988.

Clearance record

Decision date
Received
(198 days to decision)
Product code
EWO Audiometer
Regulation
21 CFR 874.1050
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Amplus Corp. 65 Bristlecone Way, Boulder CO
Third party review
No

Clearances, product code EWO

Trailing 12 months

FDA records hold no clearances under product code EWO in the trailing twelve months.

FDA records show no clearances under product code EWO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EWO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260