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FDA 510(k)

HAND HELD MEDISPACER

K-Number: K972237 · 1997-07-31

ApplicantThayer Medical Corp.
Decision Date1997-07-31
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

HAND HELD MEDISPACER 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 1997-07-31 under 510(k) number K972237. 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 HAND HELD MEDISPACER?

HAND HELD MEDISPACER is a medical device that received FDA 510(k) clearance on 1997-07-31. The listed applicant is Thayer Medical Corp.. The 510(k) number is K972237.

When did HAND HELD MEDISPACER receive FDA 510(k) clearance?

HAND HELD MEDISPACER received FDA 510(k) clearance on 1997-07-31, under 510(k) number K972237.

Who is the listed applicant for HAND HELD MEDISPACER?

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 HAND HELD MEDISPACER?

The FDA product code for HAND HELD MEDISPACER is CAF.

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Other records listing Thayer Medical Corp. as applicant

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.

K102658MINISPACER DUAL-SPRAY MDI ADAPTER WITH 22MM (OR 15MM) OD / 22MM OD/ID CONNECTIONS / 15MM ID CONNECTIONSK993101LITEAIREK992722PRIMEAIREK955805DUAL SPRAY MINISPACERK941026THAYER MASK TO MOUTHPIECE ADAPTER/CONNECTORK924535THAYER HAND HELD M.K.I. HOLDING CHAMBER

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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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