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FDA 510(k)

MOSQUITO

K-Number: K771013 · 1977-07-01

ApplicantEmde Corp.
Decision Date1977-07-01
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOSQUITO is the device name listed in this FDA 510(k) record. The listed applicant is Emde Corp.. It received FDA 510(k) clearance on 1977-07-01 under 510(k) number K771013. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOSQUITO?

MOSQUITO is a medical device that received FDA 510(k) clearance on 1977-07-01. The listed applicant is Emde Corp.. The 510(k) number is K771013.

When did MOSQUITO receive FDA 510(k) clearance?

MOSQUITO received FDA 510(k) clearance on 1977-07-01, under 510(k) number K771013.

Who is the listed applicant for MOSQUITO?

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?

The FDA product code for MOSQUITO 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K860052QWIK-CALLK811199MARZ-175K791465MOSQUITO ARTERIAL BLOOD SAMPLER

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.

K071269HEMODRAW ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K070340SECURE ARTERIAL BLOOD SAMPLING SYSTEMSmiths Medical Asd, Inc.K955663ABC IN-LINE BLOOD SAMPLING KITUtah Medical Products, Inc.K954015ABG POINT LOK NEEDLE PROTECTION DEVICEDevon Industries, Inc.K954035ACTI-FLEX ARTERIAL EXTENSION SETR-Group Intl.K950098NEEDLE SAFETY COVERHammer-Plane, Inc.

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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