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FDA 510(k)

QUICK CONNECT T ADAPTOR

K-Number: K882341 · 1988-07-18

ApplicantThayer Medical Corp.
Decision Date1988-07-18
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

QUICK CONNECT T ADAPTOR 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 1988-07-18 under 510(k) number K882341. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK CONNECT T ADAPTOR?

QUICK CONNECT T ADAPTOR is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Thayer Medical Corp.. The 510(k) number is K882341.

When did QUICK CONNECT T ADAPTOR receive FDA 510(k) clearance?

QUICK CONNECT T ADAPTOR received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882341.

Who is the listed applicant for QUICK CONNECT T ADAPTOR?

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 QUICK CONNECT T ADAPTOR?

The FDA product code for QUICK CONNECT T ADAPTOR is BZO.

Related Clinical Trials

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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: BZO)

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.

K953784UNICOR, INC. CORRUGATED TUBINGUnicor, Inc.K953785UNICOR, INC. VENTILATOR HOSESUnicor, Inc.K952010PRIMA VENTILATOR HOSESPrima, Inc.K952022PRIMA VOLUMN VENTILATORSSPrima, Inc.K952011PRIMA BREATHING BAGSPrima, Inc.K952012PRIMA CUSTOM ANESTESIA CIRCUITPrima, 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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