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FDA 510(k)

HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE

K-Number: K883481 · 1988-11-04

ApplicantHewlett-Packard Co.
Decision Date1988-11-04
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE 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 1988-11-04 under 510(k) number K883481. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE?

HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE is a medical device that received FDA 510(k) clearance on 1988-11-04. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K883481.

When did HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE receive FDA 510(k) clearance?

HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE received FDA 510(k) clearance on 1988-11-04, under 510(k) number K883481.

Who is the listed applicant for HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE?

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 HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE?

The FDA product code for HP 77025A/77030A ULTRA. SYSTEM/HP 77020CV UPGRADE is IYO.

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Other records listing Hewlett-Packard Co. 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.

K992543HEARTSTREAM XLT DEFIBRILLATOR/MONITOR, AC CHARGER, DC CHARGER, DATA CARD, SINGLE BAY ADAPTER, DEFIBRILLATOR PADS CABLEK993587HP M2376A DEVICE LINK SYSTEMK993169MODIFICATION OF: PHYSIOLOGICAL SIGNAL TRANSMITTER AND RECEIVER, MODEL 3810AK992977HEWLETT PACKARD MULTIFUNCTION PEDIATRIC DEFIB FUNCTION, MODEL M3503A & M3504AK993516HP M2600A VIRIDIA TELEMETRY SYSTEMK993171HP VIRIDIA INFORMATION SYSTEM, MODELS M3150A/ M3151A/ M3153A/ M3154A

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Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, Inc.

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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