MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)
K-Number: K971910 · 1998-03-23
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Device Summary
Frequently Asked Questions
What is the MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)?
MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A) is a medical device that received FDA 510(k) clearance on 1998-03-23. The listed applicant is Hewlett-Packard GmbH. The 510(k) number is K971910.
When did MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A) receive FDA 510(k) clearance?
MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A) received FDA 510(k) clearance on 1998-03-23, under 510(k) number K971910.
Who is the listed applicant for MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)?
The FDA 510(k) record lists Hewlett-Packard GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A)?
The FDA product code for MULTI-PARAMETER MODULE (M3000A)/DISPLAY UNIT (M3046A) 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 GmbH 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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