Airwatch II Zone

FDA 510(k) K982676 · Enact Health Management Systems

Substantially Equivalent

510(k) numberK982676

Submission

Device name
Airwatch II Zone
Applicant
Enact Health Management Systems
Mountain View, CA, US
Received
July 31, 1998
Decision date
October 29, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary 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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More from Guangzhou Homesun Medical Technology Co., Ltd.

510(k)DeviceDecision
K982675Airwatch II ZonelessBZH · Traditional 10/29/1998SE
K941226Airwatch MonitorBZH · Traditional 11/16/1994SE

Questions and answers

When was Airwatch II Zone cleared by the FDA?

Airwatch II Zone (K982676) received a 510(k) decision of Substantially Equivalent on October 29, 1998, 90 days after the submission was received.

What is the product code of K982676?

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