Pro-Flow Multipurpose Cannula

FDA 510(k) K053063 · Pro-Tech Services, Inc.

Substantially Equivalent

510(k) numberK053063

Submission

Device name
Pro-Flow Multipurpose Cannula
Applicant
Pro-Tech Services, Inc.
Mukilteo, WA, US
Received
November 1, 2005
Decision date
December 13, 2005
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1400
Specialty
Anesthesiology

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Questions and answers

When was Pro-Flow Multipurpose Cannula cleared by the FDA?

Pro-Flow Multipurpose Cannula (K053063) received a 510(k) decision of Substantially Equivalent on December 13, 2005, 42 days after the submission was received.

What is the product code of K053063?

The FDA product code is CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, a Class II (moderate risk) device regulated under 21 CFR 868.1400.