Dispossable Suction Tube, 6 French

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K791846 ↗

FDA Product Code

DTS

Device Class

Class II

Regulation

21 CFR Part 870.4420

Advisory Committee

Cardiovascular

FDA Decision

SESE Substantially Equivalent

• Infant Vent Catheter 12001 W/Side Vent Open recall

  Class II

  FDA 510(k) K834039 Active Cleared 3 Jan 1984

• Submission Coronary Cannula

  Class II

  FDA 510(k) K821149 Active Cleared 18 May 1982

• Percutaneous Guidewire Placement Syringe 50505

  Class II

  FDA 510(k) K855089 Active Cleared 18 Feb 1986

• Clearview Blower/Mister Open recall

  Class II

  FDA 510(k) K973485 Active Cleared 8 Dec 1997

• Aortic Root Cannula W/Integral Press

  Class II

  FDA 510(k) K831591 Active Cleared 30 Jun 1983

• Code #94315 Retrograde Coronary Sinus Perf Cannula

  Class II

  FDA 510(k) K901074 Active Cleared 6 Jul 1990

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