Confluent Surgical Dual Liquid Applicator, Model 70-2005-093

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K061183 ↗

FDA Product Code

FMF

FDA applicant

Confluent Surgical,Inc

Device Class

Class II

Regulation

21 CFR Part 880.5860

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Modification to Confluent Surgical Micromyst Applicator and Air Pump

  Class II

  FDA 510(k) K070814 Active Cleared 30 May 2007

• Covidien Extended Tip Applicator Open recall

  Class II

  FDA 510(k) K091315 Active Cleared 5 Jun 2009

• Confluent Surgical Micromyst Applicator and Air Pump, Models 20-5000, AP-A-6063

  Class II

  FDA 510(k) K050998 Active Cleared 15 Jun 2005

• Confluent Surgical Extended Tip Applicator, Model 70-2008-008

  Class II

  FDA 510(k) K072790 Active Cleared 11 Jan 2008

• Confluent Surgical Dual Liquid Applicator, Model 70-2005093

  Class II

  FDA 510(k) K042588 Active Cleared 9 Dec 2004