FDA 510(k)

CHESTAC-25F SPIROMETER

K-Number: K840908 · 1984-05-14

ApplicantMedical Equipment Designs, Inc.

Decision Date1984-05-14

Product CodeBZG

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

CHESTAC-25F SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Equipment Designs, Inc.. It received FDA 510(k) clearance on 1984-05-14 under 510(k) number K840908. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHESTAC-25F SPIROMETER?

CHESTAC-25F SPIROMETER is a medical device that received FDA 510(k) clearance on 1984-05-14. The listed applicant is Medical Equipment Designs, Inc.. The 510(k) number is K840908.

When did CHESTAC-25F SPIROMETER receive FDA 510(k) clearance?

CHESTAC-25F SPIROMETER received FDA 510(k) clearance on 1984-05-14, under 510(k) number K840908.

Who is the listed applicant for CHESTAC-25F SPIROMETER?

The FDA 510(k) record lists Medical Equipment Designs, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHESTAC-25F SPIROMETER?

The FDA product code for CHESTAC-25F SPIROMETER is BZG.

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Related Devices (Code: BZG)

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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.