510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K910509Substantially Equivalent

Patient Gas Sampling Line for Ohmeda 6000

Intertech Resources, Inc., Fort Myers FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K910509 is the FDA 510(k) clearance record for PATIENT GAS SAMPLING LINE FOR OHMEDA 6000, a class II device, cleared for Intertech Resources, Inc. on under FDA product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). FDA records list 29 510(k) clearances for Intertech Resources, Inc., from to . As of , FDA records show no recalls naming K910509.

Clearance record

Decision date
Received
(71 days to decision)
Product code
CCK Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Regulation
21 CFR 868.1400
Device class
Class II
Review panel
Anesthesiology
Applicant
Intertech Resources, Inc. 5100 Tice St., Fort Myers FL
Third party review
No

Clearances, product code CCK

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