MDM ARTERIAL BLOOD GAS SYRINGE
K-Number: K812560 · 1981-10-09
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Device Summary
Frequently Asked Questions
What is the MDM ARTERIAL BLOOD GAS SYRINGE?
MDM ARTERIAL BLOOD GAS SYRINGE is a medical device that received FDA 510(k) clearance on 1981-10-09. The listed applicant is Martell Medical Products, Inc.. The 510(k) number is K812560.
When did MDM ARTERIAL BLOOD GAS SYRINGE receive FDA 510(k) clearance?
MDM ARTERIAL BLOOD GAS SYRINGE received FDA 510(k) clearance on 1981-10-09, under 510(k) number K812560.
Who is the listed applicant for MDM ARTERIAL BLOOD GAS SYRINGE?
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 SYRINGE?
The FDA product code for MDM ARTERIAL BLOOD GAS SYRINGE 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.
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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