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FDA 510(k)

NON-INVASIVE AUTOMATIC BLOOD PRESSURE

K-Number: K821378 · 1982-07-08

ApplicantNarco Scientific
Decision Date1982-07-08
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NON-INVASIVE AUTOMATIC BLOOD PRESSURE is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1982-07-08 under 510(k) number K821378. 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 NON-INVASIVE AUTOMATIC BLOOD PRESSURE?

NON-INVASIVE AUTOMATIC BLOOD PRESSURE is a medical device that received FDA 510(k) clearance on 1982-07-08. The listed applicant is Narco Scientific. The 510(k) number is K821378.

When did NON-INVASIVE AUTOMATIC BLOOD PRESSURE receive FDA 510(k) clearance?

NON-INVASIVE AUTOMATIC BLOOD PRESSURE received FDA 510(k) clearance on 1982-07-08, under 510(k) number K821378.

Who is the listed applicant for NON-INVASIVE AUTOMATIC BLOOD PRESSURE?

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

What is the FDA product code for NON-INVASIVE AUTOMATIC BLOOD PRESSURE?

The FDA product code for NON-INVASIVE AUTOMATIC BLOOD PRESSURE is DXN.

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Other records listing Narco Scientific 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.

K830338NARCOTRACE 80K831429AS 191 ECG TELEMETRY MODULEK831428AS 1740 INTERFACE MODULEK822835PZ-800 VOLUME VENTILATORK831430AIR SHIELDS AS-100 MONIORING SYS-AS105K831460AS 30/TCP MODULE

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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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