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FDA 510(k)

THORATEC GAS SAMPLING CONNECTOR

K-Number: K822769 · 1982-10-06

ApplicantThoratec Laboratories Corp.
Decision Date1982-10-06
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THORATEC GAS SAMPLING CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Thoratec Laboratories Corp.. It received FDA 510(k) clearance on 1982-10-06 under 510(k) number K822769. 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 THORATEC GAS SAMPLING CONNECTOR?

THORATEC GAS SAMPLING CONNECTOR is a medical device that received FDA 510(k) clearance on 1982-10-06. The listed applicant is Thoratec Laboratories Corp.. The 510(k) number is K822769.

When did THORATEC GAS SAMPLING CONNECTOR receive FDA 510(k) clearance?

THORATEC GAS SAMPLING CONNECTOR received FDA 510(k) clearance on 1982-10-06, under 510(k) number K822769.

Who is the listed applicant for THORATEC GAS SAMPLING CONNECTOR?

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

What is the FDA product code for THORATEC GAS SAMPLING CONNECTOR?

The FDA product code for THORATEC GAS SAMPLING CONNECTOR is CAI.

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Other records listing Thoratec Laboratories 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.

K001927VECTRA (TM) VASCULAR ACCESS GRAFT-5MM DIAMETER,6MM DIAMETER AND VECTRA (TM) VASCULAR ACCESS GRAFT FOR REVISION-5MM DIAMEK001926VASCULAR GRAFT TUNNELER-STANDARD CURVE, MID CURVE, FULL CURVE, SHORT STANDARD CURVE, VASCULAR GRAFT TUNNELER ACCESSORIESK851495THORATEC MULTILUMEN CENTRAL VENOUS CATH-TRAYK833714RESPIRATORY ASSESSMENT SYSTEMK833265RESPIRATORY FLOW MODULEK831557INTRAOPERATIVE AUTOTRANSFUSION SYS

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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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