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FDA 510(k)

HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST

K-Number: K905100 · 1991-01-15

ApplicantHewlett-Packard Co.
Decision Date1991-01-15
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST 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 1991-01-15 under 510(k) number K905100. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST?

HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST is a medical device that received FDA 510(k) clearance on 1991-01-15. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K905100.

When did HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST receive FDA 510(k) clearance?

HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST received FDA 510(k) clearance on 1991-01-15, under 510(k) number K905100.

Who is the listed applicant for HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST?

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 HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST?

The FDA product code for HEWLETT PACKARD MODEL 5650C, CARDIO DATA MGMT SYST is DQK.

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Other records listing Hewlett-Packard Co. as applicant

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Related Devices (Code: DQK)

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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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