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FDA 510(k)

MEDDORNA WIRELESS PRN SPIROMETER 100

K-Number: K072722 · 2008-04-24

ApplicantMeddorna, LLC
Decision Date2008-04-24
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDDORNA WIRELESS PRN SPIROMETER 100 is the device name listed in this FDA 510(k) record. The listed applicant is Meddorna, LLC. It received FDA 510(k) clearance on 2008-04-24 under 510(k) number K072722. 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 MEDDORNA WIRELESS PRN SPIROMETER 100?

MEDDORNA WIRELESS PRN SPIROMETER 100 is a medical device that received FDA 510(k) clearance on 2008-04-24. The listed applicant is Meddorna, LLC. The 510(k) number is K072722.

When did MEDDORNA WIRELESS PRN SPIROMETER 100 receive FDA 510(k) clearance?

MEDDORNA WIRELESS PRN SPIROMETER 100 received FDA 510(k) clearance on 2008-04-24, under 510(k) number K072722.

Who is the listed applicant for MEDDORNA WIRELESS PRN SPIROMETER 100?

The FDA 510(k) record lists Meddorna, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDDORNA WIRELESS PRN SPIROMETER 100?

The FDA product code for MEDDORNA WIRELESS PRN SPIROMETER 100 is BZG.

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Related Devices (Code: BZG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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