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)

ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS

K-Number: K040286 · 2004-03-15

ApplicantEthox Corp.
Decision Date2004-03-15
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Ethox Corp.. It received FDA 510(k) clearance on 2004-03-15 under 510(k) number K040286. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS?

ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS is a medical device that received FDA 510(k) clearance on 2004-03-15. The listed applicant is Ethox Corp.. The 510(k) number is K040286.

When did ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS receive FDA 510(k) clearance?

ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS received FDA 510(k) clearance on 2004-03-15, under 510(k) number K040286.

Who is the listed applicant for ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS?

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

What is the FDA product code for ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS?

The FDA product code for ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFS is DXQ.

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 Ethox 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.

K031195CUF-COVER (TM)K962850TUM-E-VACK935633NO-MESK921946TUM-E-VAC BITE BLOCKK885220PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KITK894927SURGI SQUEEZ

View all 19 devices →

Related Devices (Code: DXQ)

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.

K254287Medline Reusable Blood Pressure CuffMedline Industries, LPK260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden CorporationK253089NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)Shenzhen Best Electronics Co., Ltd.K253964Disposable Neonatal NIBP Cuff (U1681S-C51N)Unimed Medical Supplies, Inc.K251745Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs)Baxter Healthcare CorporationK250765AViTA Arm Type Blood Pressure Monitor CuffAvita Corporation

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.

↑