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FDA 510(k)

THAYER METERED DOSE INHALER DISPENSER/ADAPTER

K-Number: K901739 · 1990-10-09

ApplicantThayer Medical Corp.
Decision Date1990-10-09
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THAYER METERED DOSE INHALER DISPENSER/ADAPTER 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 1990-10-09 under 510(k) number K901739. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THAYER METERED DOSE INHALER DISPENSER/ADAPTER?

THAYER METERED DOSE INHALER DISPENSER/ADAPTER is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Thayer Medical Corp.. The 510(k) number is K901739.

When did THAYER METERED DOSE INHALER DISPENSER/ADAPTER receive FDA 510(k) clearance?

THAYER METERED DOSE INHALER DISPENSER/ADAPTER received FDA 510(k) clearance on 1990-10-09, under 510(k) number K901739.

Who is the listed applicant for THAYER METERED DOSE INHALER DISPENSER/ADAPTER?

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 METERED DOSE INHALER DISPENSER/ADAPTER?

The FDA product code for THAYER METERED DOSE INHALER DISPENSER/ADAPTER is CAI.

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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 CONNECTIONSK993101LITEAIREK992722PRIMEAIREK972237HAND HELD MEDISPACERK955805DUAL SPRAY MINISPACERK941026THAYER MASK TO MOUTHPIECE ADAPTER/CONNECTOR

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Related Devices (Code: CAI)

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.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

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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