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FDA 510(k)

MODEL BPS08 BLOOD PRESSURE MODULE

K-Number: K881155 · 1988-07-28

ApplicantFresenius USA, Inc.
Decision Date1988-07-28
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL BPS08 BLOOD PRESSURE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is Fresenius USA, Inc.. It received FDA 510(k) clearance on 1988-07-28 under 510(k) number K881155. 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 MODEL BPS08 BLOOD PRESSURE MODULE?

MODEL BPS08 BLOOD PRESSURE MODULE is a medical device that received FDA 510(k) clearance on 1988-07-28. The listed applicant is Fresenius USA, Inc.. The 510(k) number is K881155.

When did MODEL BPS08 BLOOD PRESSURE MODULE receive FDA 510(k) clearance?

MODEL BPS08 BLOOD PRESSURE MODULE received FDA 510(k) clearance on 1988-07-28, under 510(k) number K881155.

Who is the listed applicant for MODEL BPS08 BLOOD PRESSURE MODULE?

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

What is the FDA product code for MODEL BPS08 BLOOD PRESSURE MODULE?

The FDA product code for MODEL BPS08 BLOOD PRESSURE MODULE is DXN.

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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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