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)

CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN

K-Number: K884991 · 1989-06-06

ApplicantDatex Division Instrumentarium Corp.
Decision Date1989-06-06
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN is the device name listed in this FDA 510(k) record. The listed applicant is Datex Division Instrumentarium Corp.. It received FDA 510(k) clearance on 1989-06-06 under 510(k) number K884991. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN?

CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN is a medical device that received FDA 510(k) clearance on 1989-06-06. The listed applicant is Datex Division Instrumentarium Corp.. The 510(k) number is K884991.

When did CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN receive FDA 510(k) clearance?

CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN received FDA 510(k) clearance on 1989-06-06, under 510(k) number K884991.

Who is the listed applicant for CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN?

The FDA 510(k) record lists Datex Division Instrumentarium Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN?

The FDA product code for CARDIOCAP CCK-104 KEYBOARD & CCP-104 GRAPHICS PRIN is BSZ.

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 Datex Division Instrumentarium 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.

K953175AS/3 ESTPR MODULEK961247AS/3 LIGHT MONITORK943458AS/3 AIRWAY MODULEK945234AS/3 MEMORY MODULE, M0MEMK933156DATEX AS/3 PATIENT MONITORK933285DATEX AS/3 TM ANAESTHESIA MONITOR

View all 55 devices →

Related Devices (Code: BSZ)

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.

K253330A5 Anesthesia System (A5); A7 Anesthesia System (A7)Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K252746Atlan (A100); Atlan (A100 XL); Atlan(A350); Atlan (A350 XL)Drägerwerk AG Co. KgaaK251352Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-700i and related 610i, 620i, 630i series enabled to retrofit RFID features); Codonics Safe Labeling System-Point of Care Station (PCS) (SLS-1, SLS XXX, Multiple Models Pending Configuration)Codonics.IncorporatedK230931AtlanDrägerwerk AG Co. KgaaK213867Carestation 750/750cDatex-Ohmeda, Inc.K201957A8, A9 Anesthesia SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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.

↑