MOSQUITO ARTERIAL BLOOD SAMPLER
K-Number: K791465 · 1979-09-17
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Device Summary
Frequently Asked Questions
What is the MOSQUITO ARTERIAL BLOOD SAMPLER?
MOSQUITO ARTERIAL BLOOD SAMPLER is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Emde Corp.. The 510(k) number is K791465.
When did MOSQUITO ARTERIAL BLOOD SAMPLER receive FDA 510(k) clearance?
MOSQUITO ARTERIAL BLOOD SAMPLER received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791465.
Who is the listed applicant for MOSQUITO ARTERIAL BLOOD SAMPLER?
The FDA 510(k) record lists Emde Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOSQUITO ARTERIAL BLOOD SAMPLER?
The FDA product code for MOSQUITO ARTERIAL BLOOD SAMPLER is CBT.
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 Emde Corp. 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: 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.
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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