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FDA 510(k)

MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A

K-Number: K910490 · 1991-04-26

Decision Date1991-04-26
Product CodeDSI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A 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 1991-04-26 under 510(k) number K910490. The device is classified under product code DSI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A?

MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A is a medical device that received FDA 510(k) clearance on 1991-04-26. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K910490.

When did MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A receive FDA 510(k) clearance?

MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A received FDA 510(k) clearance on 1991-04-26, under 510(k) number K910490.

Who is the listed applicant for MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A?

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 MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A?

The FDA product code for MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A is DSI.

Related Clinical Trials

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.

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.

View all 230 devices →

Related Devices (Code: DSI)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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