510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930203Substantially Equivalent

Model 322 Clinical Audiometer

Virtual Corp., Portland OR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930203 is the FDA 510(k) clearance record for MODEL 322 CLINICAL AUDIOMETER, cleared for Virtual Corp. on under FDA product code EWD (Protector, Hearing (Insert)). FDA records list 9 510(k) clearances for Virtual Corp., from to . As of , FDA records show no recalls naming K930203.

Clearance record

Decision date
Received
(175 days to decision)
Product code
EWD Protector, Hearing (Insert)
Device class
Unclassified
Review panel
Unknown
Applicant
Virtual Corp. 521 SW 11th, Portland OR
510(k) summary
Statement
Third party review
No

Clearances, product code EWD

Trailing 12 months

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

FDA records show no clearances under product code EWD in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EWD, 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