FDA 510(k)

ULTRASOUND 77030 IMAGING SYSTEM

K-Number: K944048 · 1995-03-01

Decision Date1995-03-01

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ULTRASOUND 77030 IMAGING SYSTEM 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 1995-03-01 under 510(k) number K944048. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRASOUND 77030 IMAGING SYSTEM?

ULTRASOUND 77030 IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1995-03-01. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K944048.

When did ULTRASOUND 77030 IMAGING SYSTEM receive FDA 510(k) clearance?

ULTRASOUND 77030 IMAGING SYSTEM received FDA 510(k) clearance on 1995-03-01, under 510(k) number K944048.

Who is the listed applicant for ULTRASOUND 77030 IMAGING SYSTEM?

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 ULTRASOUND 77030 IMAGING SYSTEM?

The FDA product code for ULTRASOUND 77030 IMAGING SYSTEM is IYN.

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: IYN)

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.