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FDA 510(k)

ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM

K-Number: K945719 · 1995-03-16

ApplicantSherwood Medical Co.
Decision Date1995-03-16
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1995-03-16 under 510(k) number K945719. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM?

ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM is a medical device that received FDA 510(k) clearance on 1995-03-16. The listed applicant is Sherwood Medical Co.. The 510(k) number is K945719.

When did ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM receive FDA 510(k) clearance?

ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM received FDA 510(k) clearance on 1995-03-16, under 510(k) number K945719.

Who is the listed applicant for ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM?

The FDA product code for ASPIR-PULSE(TM) ARTERIAL BLOOD GAS (ABG) SYSTEM is CBT.

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Other records listing Sherwood Medical Co. 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.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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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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