BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES
K-Number: K003732 · 2001-05-16
Device Summary
Frequently Asked Questions
What is the BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES?
BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES is a medical device that received FDA 510(k) clearance on 2001-05-16. The listed applicant is Braun GmbH. The 510(k) number is K003732.
When did BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES receive FDA 510(k) clearance?
BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES received FDA 510(k) clearance on 2001-05-16, under 510(k) number K003732.
Who is the listed applicant for BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES?
The FDA 510(k) record lists Braun GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES?
The FDA product code for BRAUN PRECISION SENSOR, MODEL BP 2000 SERIES is DXN.
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 Braun 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: DXN)
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.