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FDA 510(k)

THAYER EXPANSION CHAMBER METERED DOSE INHALER

K-Number: K914283 · 1992-02-26

ApplicantThayer Medical Corp.
Decision Date1992-02-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THAYER EXPANSION CHAMBER METERED DOSE INHALER 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 1992-02-26 under 510(k) number K914283. 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 THAYER EXPANSION CHAMBER METERED DOSE INHALER?

THAYER EXPANSION CHAMBER METERED DOSE INHALER is a medical device that received FDA 510(k) clearance on 1992-02-26. The listed applicant is Thayer Medical Corp.. The 510(k) number is K914283.

When did THAYER EXPANSION CHAMBER METERED DOSE INHALER receive FDA 510(k) clearance?

THAYER EXPANSION CHAMBER METERED DOSE INHALER received FDA 510(k) clearance on 1992-02-26, under 510(k) number K914283.

Who is the listed applicant for THAYER EXPANSION CHAMBER METERED DOSE INHALER?

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 THAYER EXPANSION CHAMBER METERED DOSE INHALER?

The FDA product code for THAYER EXPANSION CHAMBER METERED DOSE INHALER is CAF.

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Other records listing Thayer Medical Corp. as applicant

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Related Devices (Code: CAF)

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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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