Truezone Peak Flow Meter

FDA 510(k) K023097 · Monaghan Medical Corp.

Substantially Equivalent

510(k) numberK023097

Submission

Device name
Truezone Peak Flow Meter
Applicant
Monaghan Medical Corp.
Plattsburgh, NY, US
Received
September 18, 2002
Decision date
March 7, 2003
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BZH – Meter, Peak Flow, Spirometry
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1860
Specialty
Anesthesiology

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Questions and answers

When was Truezone Peak Flow Meter cleared by the FDA?

Truezone Peak Flow Meter (K023097) received a 510(k) decision of Substantially Equivalent on March 7, 2003, 170 days after the submission was received.

What is the product code of K023097?

The FDA product code is BZH – Meter, Peak Flow, Spirometry, a Class II (moderate risk) device regulated under 21 CFR 868.1860.