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FDA 510(k)

MARK5 ARTERIAL BLOOD GAS KIT

K-Number: K841810 · 1984-07-06

Decision Date1984-07-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MARK5 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 1984-07-06 under 510(k) number K841810. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARK5 ARTERIAL BLOOD GAS KIT?

MARK5 ARTERIAL BLOOD GAS KIT is a medical device that received FDA 510(k) clearance on 1984-07-06. The listed applicant is Martell Medical Products, Inc.. The 510(k) number is K841810.

When did MARK5 ARTERIAL BLOOD GAS KIT receive FDA 510(k) clearance?

MARK5 ARTERIAL BLOOD GAS KIT received FDA 510(k) clearance on 1984-07-06, under 510(k) number K841810.

Who is the listed applicant for MARK5 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 MARK5 ARTERIAL BLOOD GAS KIT?

The FDA product code for MARK5 ARTERIAL BLOOD GAS KIT is FMF.

Related Clinical Trials

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.

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.

View all 7 devices →

Related Devices (Code: FMF)

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.

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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