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FDA 510(k)

LITEAIRE

K-Number: K993101 · 2000-10-26

ApplicantThayer Medical Corp.
Decision Date2000-10-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LITEAIRE is the device name listed in this FDA 510(k) record. The listed applicant is Thayer Medical Corp.. It received FDA 510(k) clearance on 2000-10-26 under 510(k) number K993101. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LITEAIRE?

LITEAIRE is a medical device that received FDA 510(k) clearance on 2000-10-26. The listed applicant is Thayer Medical Corp.. The 510(k) number is K993101.

When did LITEAIRE receive FDA 510(k) clearance?

LITEAIRE received FDA 510(k) clearance on 2000-10-26, under 510(k) number K993101.

Who is the listed applicant for LITEAIRE?

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

What is the FDA product code for LITEAIRE?

The FDA product code for LITEAIRE is CAF.

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Related Devices (Code: CAF)

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

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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