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FDA 510(k)

TONOTEST BLOOD PRESSURE MONITOR

K-Number: K800904 · 1980-06-04

ApplicantRetlif, Inc.
Decision Date1980-06-04
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TONOTEST BLOOD PRESSURE MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Retlif, Inc.. It received FDA 510(k) clearance on 1980-06-04 under 510(k) number K800904. 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 TONOTEST BLOOD PRESSURE MONITOR?

TONOTEST BLOOD PRESSURE MONITOR is a medical device that received FDA 510(k) clearance on 1980-06-04. The listed applicant is Retlif, Inc.. The 510(k) number is K800904.

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

TONOTEST BLOOD PRESSURE MONITOR received FDA 510(k) clearance on 1980-06-04, under 510(k) number K800904.

Who is the listed applicant for TONOTEST BLOOD PRESSURE MONITOR?

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

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

The FDA product code for TONOTEST BLOOD PRESSURE MONITOR 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 Retlif, 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.

K812503BOSCH HEARING INSTRUMENTS

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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