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FDA 510(k)

MONITOR, PATIENT (MODEL 78331A)

K-Number: K760150 · 1976-07-19

ApplicantHewlett-Packard Co.
Decision Date1976-07-19
Product CodeDPS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MONITOR, PATIENT (MODEL 78331A) 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 1976-07-19 under 510(k) number K760150. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MONITOR, PATIENT (MODEL 78331A)?

MONITOR, PATIENT (MODEL 78331A) is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K760150.

When did MONITOR, PATIENT (MODEL 78331A) receive FDA 510(k) clearance?

MONITOR, PATIENT (MODEL 78331A) received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760150.

Who is the listed applicant for MONITOR, PATIENT (MODEL 78331A)?

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 MONITOR, PATIENT (MODEL 78331A)?

The FDA product code for MONITOR, PATIENT (MODEL 78331A) is DPS.

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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: DPS)

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.

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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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