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FDA 510(k)

CLINIFLO INCENTIVE SPIROMETER

K-Number: K003146 · 2000-11-21

ApplicantDhd Healthcare Corp.
Decision Date2000-11-21
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CLINIFLO INCENTIVE SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Dhd Healthcare Corp.. It received FDA 510(k) clearance on 2000-11-21 under 510(k) number K003146. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLINIFLO INCENTIVE SPIROMETER?

CLINIFLO INCENTIVE SPIROMETER is a medical device that received FDA 510(k) clearance on 2000-11-21. The listed applicant is Dhd Healthcare Corp.. The 510(k) number is K003146.

When did CLINIFLO INCENTIVE SPIROMETER receive FDA 510(k) clearance?

CLINIFLO INCENTIVE SPIROMETER received FDA 510(k) clearance on 2000-11-21, under 510(k) number K003146.

Who is the listed applicant for CLINIFLO INCENTIVE SPIROMETER?

The FDA 510(k) record lists Dhd Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CLINIFLO INCENTIVE SPIROMETER?

The FDA product code for CLINIFLO INCENTIVE SPIROMETER is BWF.

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Other records listing Dhd Healthcare Corp. as applicant

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Related Devices (Code: BWF)

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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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