K Number
K980550
Device Name
WHISTLE WATCH
Date Cleared
1998-08-27

(196 days)

Product Code
Regulation Number
868.1860
Panel
AN
Reference & Predicate Devices
N/A
Predicate For
N/A
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview
Intended Use

The Whistle Watch is a peak flow meter that has been designed to enable asthmatic children to check their respiratory status.

Device Description

The Whistle Watch is a peak flow meter

AI/ML Overview

I am sorry, but the provided text is a 510(k) clearance letter from the FDA for a device called "Whistle Watch." It states that the device is substantially equivalent to legally marketed predicate devices and can therefore be marketed.

However, this document does not contain any information about acceptance criteria, device performance studies, sample sizes, expert qualifications, or ground truth establishment. It is a regulatory approval document, not a study report.

Therefore, I cannot fulfill your request to describe the acceptance criteria and the study that proves the device meets them based on the given input.

§ 868.1860 Peak-flow meter for spirometry.

(a)
Identification. A peak-flow meter for spirometry is a device used to measure a patient's maximum ventilatory flow rate.(b)
Classification. Class II (performance standards).