510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K092429Substantially Equivalent

Endogator

Byrne Medical, Inc., Conroe TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K092429 is the FDA 510(k) clearance record for ENDOGATOR, a class II device, cleared for Byrne Medical, Inc. on under FDA product code FEQ (Pump, Air, Non-Manual, For Endoscope). FDA records list 12 510(k) clearances for Byrne Medical, Inc., from to . As of , FDA records show no recalls naming K092429.

Clearance record

Decision date
Received
(104 days to decision)
Product code
FEQ Pump, Air, Non-Manual, For Endoscope
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Byrne Medical, Inc. 3150 Pollock Dr., Conroe TX
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code FEQ

Trailing 12 months

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

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