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FDA 510(k)

MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT

K-Number: K974087 · 1998-06-15

ApplicantHewlett-Packard Co.
Decision Date1998-06-15
Product CodeLOS
DecisionSubstantially Equivalent

Device Summary

MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT 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 1998-06-15 under 510(k) number K974087. The device is classified under product code LOS. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT?

MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT is a medical device that received FDA 510(k) clearance on 1998-06-15. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K974087.

When did MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT receive FDA 510(k) clearance?

MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT received FDA 510(k) clearance on 1998-06-15, under 510(k) number K974087.

Who is the listed applicant for MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT?

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 MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT?

The FDA product code for MODEL M1792A THROMBOLYTIC PREDICTIVE INSTRUMENT 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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