Disposable Pressure Manometer

FDA 510(k) K140370 · Besmed Health Business Corp

Substantially Equivalent

510(k) numberK140370

Submission

Device name
Disposable Pressure Manometer
Applicant
Besmed Health Business Corp
New Taipei City, Wu-Ku District, TW
Received
February 14, 2014
Decision date
June 19, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAP – Monitor, Airway Pressure (Includes Gauge And/Or Alarm)
Device class
Class II (moderate risk)
Regulation
21 CFR 868.2600
Specialty
Anesthesiology

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Questions and answers

When was Disposable Pressure Manometer cleared by the FDA?

Disposable Pressure Manometer (K140370) received a 510(k) decision of Substantially Equivalent on June 19, 2014, 125 days after the submission was received.

What is the product code of K140370?

The FDA product code is CAP – Monitor, Airway Pressure (Includes Gauge And/Or Alarm), a Class II (moderate risk) device regulated under 21 CFR 868.2600.