510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K895359Substantially Equivalent

Adms Multiplane Rectal Probe

Avalon Technology Corp., Indianapolis IN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K895359 is the FDA 510(k) clearance record for ADMS MULTIPLANE RECTAL PROBE, a class II device, cleared for Avalon Technology Corp. on under FDA product code ITX (Transducer, Ultrasonic, Diagnostic). FDA records list 2 510(k) clearances for Avalon Technology Corp., from to . As of , FDA records show no recalls naming K895359.

Clearance record

Decision date
Received
(86 days to decision)
Product code
ITX Transducer, Ultrasonic, Diagnostic
Regulation
21 CFR 892.1570
Device class
Class II
Review panel
Radiology
Applicant
Avalon Technology Corp. 9174 Castlegate Dr., Indianapolis IN
Third party review
No

Clearances, product code ITX

Trailing 12 months
6 clearances under product code ITX in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code ITX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20263
August 20262
September 20261
October 20260