HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS
K-Number: K901252 · 1990-07-31
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Device Summary
Frequently Asked Questions
What is the HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS?
HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K901252.
When did HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS receive FDA 510(k) clearance?
HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS received FDA 510(k) clearance on 1990-07-31, under 510(k) number K901252.
Who is the listed applicant for HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS?
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 SERIES OF DISPOSABLE NIBP CUFFS?
The FDA product code for HEWLETT-PACKARD SERIES OF DISPOSABLE NIBP CUFFS is DXQ.
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: DXQ)
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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