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FDA 510(k)

PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO

K-Number: K954980 · 1996-05-15

ApplicantHewlett-Packard Co.
Decision Date1996-05-15
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO 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 1996-05-15 under 510(k) number K954980. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO?

PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO is a medical device that received FDA 510(k) clearance on 1996-05-15. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K954980.

When did PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO receive FDA 510(k) clearance?

PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO received FDA 510(k) clearance on 1996-05-15, under 510(k) number K954980.

Who is the listed applicant for PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO?

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 PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO?

The FDA product code for PAGEWRITER 200, 200I CARDIOGRAPH & INTERPRETIVE CARDIO is LOS.

Related Clinical Trials

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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 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

View all 230 devices →

Related Devices (Code: LOS)

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.

K090895EKG-PLUS II SOFTWAREBionet Co., Ltd.K083749CARDIOVIEW32 REVIEW MODULEQrs Diagnostic, LLCK073376PHILIPS ECG ALGORITHMPhilips Medical SystemsK023034CARDIOTOUCH-3000Bionet Company, Ltd.K011328CARDIO CARE EKG-2000 12-CHANNEL ELECTROCARDIOGRAPHBionet Company, Ltd.K993616CARDIO-CARD INTERPRETATION SYSTEM INasiff Assoc., 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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