EMPIRE N BLOOD PRESSURE MANOMETERS
K-Number: K002955 · 2000-12-21
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Device Summary
Frequently Asked Questions
What is the EMPIRE N BLOOD PRESSURE MANOMETERS?
EMPIRE N BLOOD PRESSURE MANOMETERS is a medical device that received FDA 510(k) clearance on 2000-12-21. The listed applicant is Rudolf Riester GmbH & Co. KG. The 510(k) number is K002955.
When did EMPIRE N BLOOD PRESSURE MANOMETERS receive FDA 510(k) clearance?
EMPIRE N BLOOD PRESSURE MANOMETERS received FDA 510(k) clearance on 2000-12-21, under 510(k) number K002955.
Who is the listed applicant for EMPIRE N BLOOD PRESSURE MANOMETERS?
The FDA 510(k) record lists Rudolf Riester GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EMPIRE N BLOOD PRESSURE MANOMETERS?
The FDA product code for EMPIRE N BLOOD PRESSURE MANOMETERS 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 Rudolf Riester GmbH & Co. KG 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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