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FDA 510(k)

TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205

K-Number: K081498 · 2008-12-17

Decision Date2008-12-17
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205 is the device name listed in this FDA 510(k) record. The listed applicant is Biocomfort Diagnostics GmbH & Co. KG. It received FDA 510(k) clearance on 2008-12-17 under 510(k) number K081498. 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 TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205?

TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205 is a medical device that received FDA 510(k) clearance on 2008-12-17. The listed applicant is Biocomfort Diagnostics GmbH & Co. KG. The 510(k) number is K081498.

When did TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205 receive FDA 510(k) clearance?

TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205 received FDA 510(k) clearance on 2008-12-17, under 510(k) number K081498.

Who is the listed applicant for TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205?

The FDA 510(k) record lists Biocomfort Diagnostics GmbH & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205?

The FDA product code for TENSO-COMFORT BLOOD PRESSURE METER, MODELS BPM 105 AND BPM 205 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.

Other records listing Biocomfort Diagnostics GmbH & Co. KG 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.

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.

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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