MARKSMAN ARTERIAL BLOOD GAS SYRINGE
K-Number: K931924 · 1993-08-03
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Device Summary
Frequently Asked Questions
What is the MARKSMAN ARTERIAL BLOOD GAS SYRINGE?
MARKSMAN ARTERIAL BLOOD GAS SYRINGE is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is Martech Medical Products, Inc.. The 510(k) number is K931924.
When did MARKSMAN ARTERIAL BLOOD GAS SYRINGE receive FDA 510(k) clearance?
MARKSMAN ARTERIAL BLOOD GAS SYRINGE received FDA 510(k) clearance on 1993-08-03, under 510(k) number K931924.
Who is the listed applicant for MARKSMAN ARTERIAL BLOOD GAS SYRINGE?
The FDA 510(k) record lists Martech Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MARKSMAN ARTERIAL BLOOD GAS SYRINGE?
The FDA product code for MARKSMAN ARTERIAL BLOOD GAS SYRINGE is JKA.
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 Martech 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: JKA)
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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