510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935059Substantially Equivalent

Insufflation Tubing Set, Phx500-082

Phx Technologies Corp., Lewisville TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935059 is the FDA 510(k) clearance record for INSUFFLATION TUBING SET, PHX500-082, a class II device, cleared for Phx Technologies Corp. on under FDA product code FCX (Insufflator, Automatic Carbon-Dioxide For Endoscope). FDA records list 49 510(k) clearances for Phx Technologies Corp., from to . As of , FDA records show no recalls naming K935059.

Clearance record

Decision date
Received
(62 days to decision)
Product code
FCX Insufflator, Automatic Carbon-Dioxide For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Phx Technologies Corp. Post Office Box 1059, Lewisville TX
510(k) summary
Statement
Third party review
No

Clearances, product code FCX

Trailing 12 months
1 clearance under product code FCX in the twelve months to October 2026, July 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FCX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20260
October 20260