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FDA 510(k)

BRAUN PRECISION SENSOR PRO, MODEL BP 2590

K-Number: K012035 · 2001-07-27

ApplicantBraun GmbH
Decision Date2001-07-27
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BRAUN PRECISION SENSOR PRO, MODEL BP 2590 is the device name listed in this FDA 510(k) record. The listed applicant is Braun GmbH. It received FDA 510(k) clearance on 2001-07-27 under 510(k) number K012035. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAUN PRECISION SENSOR PRO, MODEL BP 2590?

BRAUN PRECISION SENSOR PRO, MODEL BP 2590 is a medical device that received FDA 510(k) clearance on 2001-07-27. The listed applicant is Braun GmbH. The 510(k) number is K012035.

When did BRAUN PRECISION SENSOR PRO, MODEL BP 2590 receive FDA 510(k) clearance?

BRAUN PRECISION SENSOR PRO, MODEL BP 2590 received FDA 510(k) clearance on 2001-07-27, under 510(k) number K012035.

Who is the listed applicant for BRAUN PRECISION SENSOR PRO, MODEL BP 2590?

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 PRO, MODEL BP 2590?

The FDA product code for BRAUN PRECISION SENSOR PRO, MODEL BP 2590 is DXN.

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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.

K061351ORAL-B SONIC COMPLETEK061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESK060006BRAUN THERMOSCAN IRT 2000 INFRARED EAR THERMOMETERK031928BRAUN THERMOSCAN PRO 4000 SERIES (PROFESSIONAL USE ENVIRONMENT); BRAUN THERMOSCAN IRT 4000 SERIES (HOME USE ENVIRONMENT)K003732BRAUN PRECISION SENSOR, MODEL BP 2000 SERIESK992468BRAUN THERMOSCAN PRO3000 INFARED THERMOMETER

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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.

K261929Upper Arm Blood pressure monitor (BP7155D)OMRON Healthcare, Inc.K254000Happy Health Blood Pressure MonitorHappy Health, Inc.K262658Automatic Digital Blood Pressure monitor (LD-526)Honsun (Nantong) Co., Ltd.K261394Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6186 Plus, DBP-6286B Plus, DBP-61E3 Plus, DBP-61E2 Plus, DBP-62E3B Plus, DBP-62E2B Plus)JOYTECH Healthcare Co., Ltd.K253425Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-6194-P,DBP-6294B-P,DBP-6195P,DBP-6295B-P, DBP-6196P,DBP-6296B-P,DBP-61E1-P, DBP-62E1B-P,DBP-62E3B-P,DBP-61E2-P,DBP-62E2B-P,DBP-61E3-P,DBP-6173-P,DBP-6273B-P,DBP-6179-P,DBP-6279B-P)Joytech Healthcare Co. , Ltd.K261061BP Go (BPP-855)Wellvii, Inc.

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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