MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A
K-Number: K981576 · 1998-07-17
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Device Summary
Frequently Asked Questions
What is the MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A?
MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A is a medical device that received FDA 510(k) clearance on 1998-07-17. The listed applicant is Hewlett-Packard GmbH. The 510(k) number is K981576.
When did MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A receive FDA 510(k) clearance?
MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A received FDA 510(k) clearance on 1998-07-17, under 510(k) number K981576.
Who is the listed applicant for MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL 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, MODEL M3000A & DISPLAY UNIT, MODEL M3046A?
The FDA product code for MULTI-PARAMETER MODULE, MODEL M3000A & DISPLAY UNIT, MODEL M3046A is MHX.
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: MHX)
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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