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FDA 510(k)

ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.

K-Number: K844988 · 1985-04-04

ApplicantEthox Corp.
Decision Date1985-04-04
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. is the device name listed in this FDA 510(k) record. The listed applicant is Ethox Corp.. It received FDA 510(k) clearance on 1985-04-04 under 510(k) number K844988. 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 NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.?

ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. is a medical device that received FDA 510(k) clearance on 1985-04-04. The listed applicant is Ethox Corp.. The 510(k) number is K844988.

When did ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. receive FDA 510(k) clearance?

ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. received FDA 510(k) clearance on 1985-04-04, under 510(k) number K844988.

Who is the listed applicant for ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.?

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 NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS.?

The FDA product code for ETHOX NEONATAL BLOOD PRESSURE CUFF-STERILE/DISPOS. is DXQ.

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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.

K040286ETHOX SURGI-CUF ADULT DISPOSABLE BLOOD PRESSURE CUFFSK031195CUF-COVER (TM)K962850TUM-E-VACK935633NO-MESK921946TUM-E-VAC BITE BLOCKK885220PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT

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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.

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