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FDA 510(k)

BLOOD PRESSURE MONITOR BP600X

K-Number: K834441 · 1984-05-21

ApplicantLifeline Systems, Inc.
Decision Date1984-05-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

BLOOD PRESSURE MONITOR BP600X is the device name listed in this FDA 510(k) record. The listed applicant is Lifeline Systems, Inc.. It received FDA 510(k) clearance on 1984-05-21 under 510(k) number K834441. 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 BLOOD PRESSURE MONITOR BP600X?

BLOOD PRESSURE MONITOR BP600X is a medical device that received FDA 510(k) clearance on 1984-05-21. The listed applicant is Lifeline Systems, Inc.. The 510(k) number is K834441.

When did BLOOD PRESSURE MONITOR BP600X receive FDA 510(k) clearance?

BLOOD PRESSURE MONITOR BP600X received FDA 510(k) clearance on 1984-05-21, under 510(k) number K834441.

Who is the listed applicant for BLOOD PRESSURE MONITOR BP600X?

The FDA 510(k) record lists Lifeline Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BLOOD PRESSURE MONITOR BP600X?

The FDA product code for BLOOD PRESSURE MONITOR BP600X 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.

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Other records listing Lifeline Systems, Inc. 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.

K103214M3810A PHILIPS TELEMONITORING SYSTEM WITH EDEVICE BRIDGED130K914103LIFELINE(R) PERSONAL RESPONSE SYSTEMK831638SINGLE BED ARRHYTHMIA MONITOR AM500

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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