MODIFIED MONITORING SYSTEM MODELS M1175A & M1176A
K-Number: K910490 · 1991-04-26
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Device Summary
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.
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
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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