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FDA 510(k)

MDM ARTERIAL BLOOD GAS KIT

K-Number: K822786 · 1982-10-21

ApplicantMartell Medical Products, Inc.
Decision Date1982-10-21
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MDM ARTERIAL BLOOD GAS KIT is the device name listed in this FDA 510(k) record. The listed applicant is Martell Medical Products, Inc.. It received FDA 510(k) clearance on 1982-10-21 under 510(k) number K822786. 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 MDM ARTERIAL BLOOD GAS KIT?

MDM ARTERIAL BLOOD GAS KIT is a medical device that received FDA 510(k) clearance on 1982-10-21. The listed applicant is Martell Medical Products, Inc.. The 510(k) number is K822786.

When did MDM ARTERIAL BLOOD GAS KIT receive FDA 510(k) clearance?

MDM ARTERIAL BLOOD GAS KIT received FDA 510(k) clearance on 1982-10-21, under 510(k) number K822786.

Who is the listed applicant for MDM ARTERIAL BLOOD GAS KIT?

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

What is the FDA product code for MDM ARTERIAL BLOOD GAS KIT?

The FDA product code for MDM ARTERIAL BLOOD GAS KIT is CBT.

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Other records listing Martell Medical Products, 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.

K945454LEUR TIP CAP, VLT CAP(TM)K944941PISTON SYRINGEK841810MARK5 ARTERIAL BLOOD GAS KITK822760ARTERIAL LINE KITK821096A-LINERK812560MDM ARTERIAL BLOOD GAS SYRINGE

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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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