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FDA 510(k)

DYNAPULSE 200M

K-Number: K904739 · 1991-01-08

ApplicantPulse Metric, Inc.
Decision Date1991-01-08
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DYNAPULSE 200M is the device name listed in this FDA 510(k) record. The listed applicant is Pulse Metric, Inc.. It received FDA 510(k) clearance on 1991-01-08 under 510(k) number K904739. 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 DYNAPULSE 200M?

DYNAPULSE 200M is a medical device that received FDA 510(k) clearance on 1991-01-08. The listed applicant is Pulse Metric, Inc.. The 510(k) number is K904739.

When did DYNAPULSE 200M receive FDA 510(k) clearance?

DYNAPULSE 200M received FDA 510(k) clearance on 1991-01-08, under 510(k) number K904739.

Who is the listed applicant for DYNAPULSE 200M?

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

What is the FDA product code for DYNAPULSE 200M?

The FDA product code for DYNAPULSE 200M 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 Pulse Metric, 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.

K013478DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEMK013358DYNAPULSE 5000A MINI ABP BLOOD PRESSURE MONITORING SYSTEMK012498DYNAPULSE 500G (DP500G) BLLOD PRESSURE MONITORING SYSTEMK945111DYNAPULSE 5000A (DP5000A)

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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