510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K820119Substantially Equivalent

Podioscope by Arrow

Arrow X-Ray Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820119 is the FDA 510(k) clearance record for PODIOSCOPE BY ARROW, a class II device, cleared for Arrow X-Ray Corp. on under FDA product code KPW (Device, Beam Limiting, X-Ray, Diagnostic). FDA records list 2 510(k) clearances for Arrow X-Ray Corp. As of , FDA records show no recalls naming K820119.

Clearance record

Decision date
Received
(31 days to decision)
Product code
KPW Device, Beam Limiting, X-Ray, Diagnostic
Regulation
21 CFR 892.1610
Device class
Class II
Review panel
Radiology
Applicant
Arrow X-Ray Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KPW

Trailing 12 months

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

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