Vitalograph Micro

FDA 510(k) K991412 · Vitalograph, Inc.

Substantially Equivalent

510(k) numberK991412

Submission

Device name
Vitalograph Micro
Applicant
Vitalograph, Inc.
Lenexa, KS, US
Received
April 23, 1999
Decision date
February 4, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 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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More from Guangzhou Homesun Medical Technology Co., Ltd.

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K253293VitaloJAK Clinic (Model 7100)DSH · Special 12/03/2025SE
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K943678Electronic Flow MeterBZH · Traditional 12/14/1995SE
K950854Vitalograph 2110 Software InterfaceDSH · Traditional 10/12/1995SE
K946075Vitalograph Model 2120BZG · Traditional 08/04/1995SE
K942779Disposable Bacteriological FilterBZG · Traditional 07/13/1994SE
K925085Escort SpirometerBZG · Traditional 08/12/1993SE
K930085Vitalograph Data Storage SpirometerBTY · Traditional 07/26/1993SE
K912412Vitalograph Spirotrac IIIBZG · Traditional 10/15/1991SE
K893665Aerosol Inhalation MonitorBWF · Traditional 08/21/1989SE

Questions and answers

When was Vitalograph Micro cleared by the FDA?

Vitalograph Micro (K991412) received a 510(k) decision of Substantially Equivalent on February 4, 2000, 287 days after the submission was received.

What is the product code of K991412?

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