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FDA 510(k)

MODEL M1175A/M1176A WITH ST SEGMENT MONITORING

K-Number: K900032 · 1990-04-10

ApplicantHewlett-Packard Co.
Decision Date1990-04-10
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL M1175A/M1176A WITH ST SEGMENT MONITORING 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 1990-04-10 under 510(k) number K900032. 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 MODEL M1175A/M1176A WITH ST SEGMENT MONITORING?

MODEL M1175A/M1176A WITH ST SEGMENT MONITORING is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K900032.

When did MODEL M1175A/M1176A WITH ST SEGMENT MONITORING receive FDA 510(k) clearance?

MODEL M1175A/M1176A WITH ST SEGMENT MONITORING received FDA 510(k) clearance on 1990-04-10, under 510(k) number K900032.

Who is the listed applicant for MODEL M1175A/M1176A WITH ST SEGMENT MONITORING?

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 M1175A/M1176A WITH ST SEGMENT MONITORING?

The FDA product code for MODEL M1175A/M1176A WITH ST SEGMENT MONITORING is DRT.

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Other records listing Hewlett-Packard Co. as applicant

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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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