SYRINGE, PISTON, ARTERIAL BLOOD SAMPL
K-Number: K840924 · 1984-03-23
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Device Summary
Frequently Asked Questions
What is the SYRINGE, PISTON, ARTERIAL BLOOD SAMPL?
SYRINGE, PISTON, ARTERIAL BLOOD SAMPL is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Medcare Disp Products, Inc.. The 510(k) number is K840924.
When did SYRINGE, PISTON, ARTERIAL BLOOD SAMPL receive FDA 510(k) clearance?
SYRINGE, PISTON, ARTERIAL BLOOD SAMPL received FDA 510(k) clearance on 1984-03-23, under 510(k) number K840924.
Who is the listed applicant for SYRINGE, PISTON, ARTERIAL BLOOD SAMPL?
The FDA 510(k) record lists Medcare Disp Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYRINGE, PISTON, ARTERIAL BLOOD SAMPL?
The FDA product code for SYRINGE, PISTON, ARTERIAL BLOOD SAMPL 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 Medcare Disp 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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