FDA 510(k)

ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS

K-Number: K905147 · 1990-12-27

Decision Date1990-12-27

Product CodeDXQ

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1990-12-27 under 510(k) number K905147. 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 ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS?

ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS is a medical device that received FDA 510(k) clearance on 1990-12-27. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K905147.

When did ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS receive FDA 510(k) clearance?

ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS received FDA 510(k) clearance on 1990-12-27, under 510(k) number K905147.

Who is the listed applicant for ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. CUFFS?

The FDA product code for ADULT,STERILE,DISPOS.,NONIVAS.,BLOOD PRESS. 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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hewlett-Packard Co. as applicant

K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLE K993587HP M2376A DEVICE LINK SYSTEM K993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810A K992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504A K993516HP M2600A VIRIDIA TELEMETRY SYSTEM K993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

View all 230 devices →

Related Devices (Code: DXQ)

K254287Medline Reusable Blood Pressure CuffMedline Industries, LP K260747YP-710T Series NIBP Cuff;YP-840T Series Disposable CuffNihon Kohden Corporation K253089NIBP 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 Corporation K250765AViTA 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.