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FDA 510(k)

ARGIS PULMONARY FUNCTION TESTING SYSTEM

K-Number: K883732 · 1989-03-09

ApplicantAdvanced Signal Processing, Inc.
Decision Date1989-03-09
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARGIS PULMONARY FUNCTION TESTING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Signal Processing, Inc.. It received FDA 510(k) clearance on 1989-03-09 under 510(k) number K883732. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARGIS PULMONARY FUNCTION TESTING SYSTEM?

ARGIS PULMONARY FUNCTION TESTING SYSTEM is a medical device that received FDA 510(k) clearance on 1989-03-09. The listed applicant is Advanced Signal Processing, Inc.. The 510(k) number is K883732.

When did ARGIS PULMONARY FUNCTION TESTING SYSTEM receive FDA 510(k) clearance?

ARGIS PULMONARY FUNCTION TESTING SYSTEM received FDA 510(k) clearance on 1989-03-09, under 510(k) number K883732.

Who is the listed applicant for ARGIS PULMONARY FUNCTION TESTING SYSTEM?

The FDA 510(k) record lists Advanced Signal Processing, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARGIS PULMONARY FUNCTION TESTING SYSTEM?

The FDA product code for ARGIS PULMONARY FUNCTION TESTING SYSTEM is BZC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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