Vitalograph Function Analyzer

FDA 510(k) K791503 · Vitalograph , Ltd.

Substantially Equivalent

510(k) numberK791503

Submission

Device name
Vitalograph Function Analyzer
Applicant
Vitalograph , Ltd.
Mchenry, IL, US
Received
August 8, 1979
Decision date
August 16, 1979
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BZC – Calculator, Pulmonary Function Data
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1880
Specialty
Anesthesiology

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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
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Questions and answers

When was Vitalograph Function Analyzer cleared by the FDA?

Vitalograph Function Analyzer (K791503) received a 510(k) decision of Substantially Equivalent on August 16, 1979, 8 days after the submission was received.

What is the product code of K791503?

The FDA product code is BZC – Calculator, Pulmonary Function Data, a Class II (moderate risk) device regulated under 21 CFR 868.1880.