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FDA 510(k)

INSPIRON PULMONARY FUNCTION ANALYZER

K-Number: K802920 · 1981-02-23

ApplicantC.R. Bard, Inc.
Decision Date1981-02-23
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INSPIRON PULMONARY FUNCTION ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1981-02-23 under 510(k) number K802920. 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 INSPIRON PULMONARY FUNCTION ANALYZER?

INSPIRON PULMONARY FUNCTION ANALYZER is a medical device that received FDA 510(k) clearance on 1981-02-23. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K802920.

When did INSPIRON PULMONARY FUNCTION ANALYZER receive FDA 510(k) clearance?

INSPIRON PULMONARY FUNCTION ANALYZER received FDA 510(k) clearance on 1981-02-23, under 510(k) number K802920.

Who is the listed applicant for INSPIRON PULMONARY FUNCTION ANALYZER?

The FDA 510(k) record lists C.R. Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSPIRON PULMONARY FUNCTION ANALYZER?

The FDA product code for INSPIRON PULMONARY FUNCTION ANALYZER is BZC.

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Official Source

View on FDA Database →

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

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