510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932142Substantially Equivalent

Suction Guillotine Device

Triton Technology, Inc., Salem OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932142 is the FDA 510(k) clearance record for SUCTION GUILLOTINE DEVICE, a class II device, cleared for Triton Technology, Inc. on under FDA product code FCK (Instrument, Biopsy, Suction). FDA records list 4 510(k) clearances for Triton Technology, Inc., from to . As of , FDA records show no recalls naming K932142.

Clearance record

Decision date
Received
(144 days to decision)
Product code
FCK Instrument, Biopsy, Suction
Regulation
21 CFR 876.1075
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Triton Technology, Inc. 2380 Southeast Blvd., Salem OH
510(k) summary
Statement
Third party review
No

Clearances, product code FCK

Trailing 12 months

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

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