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FDA 510(k)

PATIENT MONITOR 788 33A

K-Number: K831943 · 1983-10-19

ApplicantHewlett-Packard Co.
Decision Date1983-10-19
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PATIENT MONITOR 788 33A 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 1983-10-19 under 510(k) number K831943. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PATIENT MONITOR 788 33A?

PATIENT MONITOR 788 33A is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K831943.

When did PATIENT MONITOR 788 33A receive FDA 510(k) clearance?

PATIENT MONITOR 788 33A received FDA 510(k) clearance on 1983-10-19, under 510(k) number K831943.

Who is the listed applicant for PATIENT MONITOR 788 33A?

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 PATIENT MONITOR 788 33A?

The FDA product code for PATIENT MONITOR 788 33A is DRT.

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Other records listing Hewlett-Packard Co. as applicant

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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: DRT)

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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