Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MARQUEST MICRO STIK 9000 SERIES

K-Number: K842008 · 1984-05-25

ApplicantMarquest Medical Products, Inc.
Decision Date1984-05-25
Product CodeCBT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MARQUEST MICRO STIK 9000 SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Marquest Medical Products, Inc.. It received FDA 510(k) clearance on 1984-05-25 under 510(k) number K842008. 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 MARQUEST MICRO STIK 9000 SERIES?

MARQUEST MICRO STIK 9000 SERIES is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Marquest Medical Products, Inc.. The 510(k) number is K842008.

When did MARQUEST MICRO STIK 9000 SERIES receive FDA 510(k) clearance?

MARQUEST MICRO STIK 9000 SERIES received FDA 510(k) clearance on 1984-05-25, under 510(k) number K842008.

Who is the listed applicant for MARQUEST MICRO STIK 9000 SERIES?

The FDA 510(k) record lists Marquest Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARQUEST MICRO STIK 9000 SERIES?

The FDA product code for MARQUEST MICRO STIK 9000 SERIES 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 Marquest 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.

K050066C-CO2 COLORIMETRIC CO2 INDICATORK970478SCT 3000 HEATED HUMIDIFIERK962223WATER CHAMBERS FOR ST 3000 HEATED HUMIDIFIERK962220HEATED WIRE CIRCUITS FOR SCT 3000 HEATED HUMIDIFIERK961838RESPIRGARD II, SPIROGARDK960972DISPOSABLE GAS SAMPLING INTERFACE KITS

View all 32 devices →

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.

↑