510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K952219Substantially Equivalent

Suction Tip Cleaner Cup

Moore/Gobel, Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K952219 is the FDA 510(k) clearance record for SUCTION TIP CLEANER CUP, a class II device, cleared for Moore/Gobel on under FDA product code GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered). FDA records list one 510(k) clearance for Moore/Gobel. As of , FDA records show no recalls naming K952219.

Clearance record

Decision date
Received
(188 days to decision)
Product code
GCX Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Regulation
21 CFR 880.6740
Device class
Class II
Review panel
General Hospital
Applicant
Moore/Gobel 9712 S. Altamont Dr., Sandy UT
510(k) summary
Statement
Third party review
No

Clearances, product code GCX

Trailing 12 months

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

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