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FDA 510(k)

LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI

K-Number: K853599 · 1986-03-21

ApplicantLitton Datamedix
Decision Date1986-03-21
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI is the device name listed in this FDA 510(k) record. The listed applicant is Litton Datamedix. It received FDA 510(k) clearance on 1986-03-21 under 510(k) number K853599. 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 LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI?

LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI is a medical device that received FDA 510(k) clearance on 1986-03-21. The listed applicant is Litton Datamedix. The 510(k) number is K853599.

When did LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI receive FDA 510(k) clearance?

LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI received FDA 510(k) clearance on 1986-03-21, under 510(k) number K853599.

Who is the listed applicant for LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI?

The FDA 510(k) record lists Litton Datamedix as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI?

The FDA product code for LITTON DATAMEDIX BLOOD PRESSURE MONITOR NI 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 Litton Datamedix 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.

K850290ULTRASOUND GELK842497SERVOMED OXYMONITO SMK 363K842312SERVOCARD SCP-840K842235SERVOCARD DEFIBRILLATOR SCP-851

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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