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)

MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING

K-Number: K905464 · 1991-05-31

ApplicantAngiosystems, Inc.
Decision Date1991-05-31
Product CodeCBT
Advisory CommitteeAN
DecisionUnknown

Device Summary

MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING is the device name listed in this FDA 510(k) record. The listed applicant is Angiosystems, Inc.. It received FDA 510(k) clearance on 1991-05-31 under 510(k) number K905464. The device is classified under product code CBT. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING?

MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING is a medical device that received FDA 510(k) clearance on 1991-05-31. The listed applicant is Angiosystems, Inc.. The 510(k) number is K905464.

When did MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING receive FDA 510(k) clearance?

MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING received FDA 510(k) clearance on 1991-05-31, under 510(k) number K905464.

Who is the listed applicant for MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING?

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

What is the FDA product code for MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING?

The FDA product code for MEDICAL PROCEDURE KITS/ARTERIAL BLOOD SAMPLING 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 Angiosystems, 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.

K905459SURGICAL PROCEDURE TRAY/LAPAROSCOPY CHOLECYSTECTOMK905461PROCEDURE KIT/ROUTINE DENTAL PROCEDURESK905466STERILE DISPOSABLE SURGICAL DRAPE/ABDOMINAL DRAPEK905465STERILE DISPOS SURGICAL DRAPE/C-SECTION DRAPEK905460STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERYK905462PROCEDURE TRAY/FOR VARIOUS OPHTHALMIC PROCEDURES

View all 14 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.

↑