510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092244Substantially Equivalent

Ma61, Ma62, Ma63 Family of Portable Audiometers

Diagnostic Group LLC, Minnesota MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K092244 is the FDA 510(k) clearance record for MA61, MA62, MA63 FAMILY OF PORTABLE AUDIOMETERS, a class II device, cleared for Diagnostic Group, LLC on under FDA product code EWO (Audiometer). FDA records list one 510(k) clearance for Diagnostic Group, LLC. As of , FDA records show no recalls naming K092244.

Clearance record

Decision date
Received
(216 days to decision)
Product code
EWO Audiometer
Regulation
21 CFR 874.1050
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
Diagnostic Group, LLC 7625 Golden Triangle Dr., Minnesota MN
510(k) summary
Statement
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