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FDA 510(k)

HP M177XA CARDIOGRAPHS

K-Number: K935772 · 1994-07-26

ApplicantHewlett-Packard Co.
Decision Date1994-07-26
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

HP M177XA CARDIOGRAPHS 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 1994-07-26 under 510(k) number K935772. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HP M177XA CARDIOGRAPHS?

HP M177XA CARDIOGRAPHS is a medical device that received FDA 510(k) clearance on 1994-07-26. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K935772.

When did HP M177XA CARDIOGRAPHS receive FDA 510(k) clearance?

HP M177XA CARDIOGRAPHS received FDA 510(k) clearance on 1994-07-26, under 510(k) number K935772.

Who is the listed applicant for HP M177XA CARDIOGRAPHS?

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 M177XA CARDIOGRAPHS?

The FDA product code for HP M177XA CARDIOGRAPHS is LOS.

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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: 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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