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FDA 510(k)

IMPULSE SELECT

K-Number: K001579 · 2000-08-31

ApplicantAirsep Corp.
Decision Date2000-08-31
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IMPULSE SELECT is the device name listed in this FDA 510(k) record. The listed applicant is Airsep Corp.. It received FDA 510(k) clearance on 2000-08-31 under 510(k) number K001579. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPULSE SELECT?

IMPULSE SELECT is a medical device that received FDA 510(k) clearance on 2000-08-31. The listed applicant is Airsep Corp.. The 510(k) number is K001579.

When did IMPULSE SELECT receive FDA 510(k) clearance?

IMPULSE SELECT received FDA 510(k) clearance on 2000-08-31, under 510(k) number K001579.

Who is the listed applicant for IMPULSE SELECT?

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

What is the FDA product code for IMPULSE SELECT?

The FDA product code for IMPULSE SELECT is NFB.

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Related Devices (Code: NFB)

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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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