Medgem

FDA 510(k) K021605 · Healthetech, Inc.

Substantially Equivalent

510(k) numberK021605

Submission

Device name
Medgem
Applicant
Healthetech, Inc.
Golden, CO, US
Received
May 16, 2002
Decision date
June 14, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
BZL – Computer, Oxygen-Uptake
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1730
Specialty
Anesthesiology

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Questions and answers

When was Medgem cleared by the FDA?

Medgem (K021605) received a 510(k) decision of Substantially Equivalent on June 14, 2002, 29 days after the submission was received.

What is the product code of K021605?

The FDA product code is BZL – Computer, Oxygen-Uptake, a Class II (moderate risk) device regulated under 21 CFR 868.1730.