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FDA 510(k)

ARTERIAL BLOOD SAMPLING TRAY

K-Number: K771975 · 1977-10-28

ApplicantRespiratory Care, Inc.
Decision Date1977-10-28
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARTERIAL BLOOD SAMPLING TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K771975. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTERIAL BLOOD SAMPLING TRAY?

ARTERIAL BLOOD SAMPLING TRAY is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K771975.

When did ARTERIAL BLOOD SAMPLING TRAY receive FDA 510(k) clearance?

ARTERIAL BLOOD SAMPLING TRAY received FDA 510(k) clearance on 1977-10-28, under 510(k) number K771975.

Who is the listed applicant for ARTERIAL BLOOD SAMPLING TRAY?

The FDA 510(k) record lists Respiratory Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARTERIAL BLOOD SAMPLING TRAY?

The FDA product code for ARTERIAL BLOOD SAMPLING TRAY is CBT.

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Other records listing Respiratory Care, Inc. 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.

K892230RCI VIRAL/BACTERIAL FILTERK884150MODIFIED CONCHATHERM III CONTROLLED HEATERK881625CONCHATHERM III PLUS DUAL HEAT WIRE SERVO CONTROLLK864147AQUAVALVEK863955COLBY LEVEL ALARMK861555CIRCAPAK UNIVERSAL VOLUME VENTILATOR CIRCUIT

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Related Devices (Code: CBT)

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.

K071269HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K070340SECURE ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K955663ABC IN-LINE BLOOD SAMPLING KITUtah Medical Products, Inc.K954015ABG POINT LOK NEEDLE PROTECTION DEVICEDevon Industries, Inc.K954035ACTI-FLEX ARTERIAL EXTENSION SETR-Group Intl.K950098NEEDLE SAFETY COVERHammer-Plane, 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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