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FDA 510(k)

WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK

K-Number: K991545 · 2000-01-19

ApplicantIndustrielle Entwicklung Medizintechnik Und Vertri
Decision Date2000-01-19
Product CodeDXQ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Industrielle Entwicklung Medizintechnik Und Vertri. It received FDA 510(k) clearance on 2000-01-19 under 510(k) number K991545. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK?

WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK is a medical device that received FDA 510(k) clearance on 2000-01-19. The listed applicant is Industrielle Entwicklung Medizintechnik Und Vertri. The 510(k) number is K991545.

When did WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK receive FDA 510(k) clearance?

WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK received FDA 510(k) clearance on 2000-01-19, under 510(k) number K991545.

Who is the listed applicant for WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK?

The FDA 510(k) record lists Industrielle Entwicklung Medizintechnik Und Vertri as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK?

The FDA product code for WATCH STYLE WRIST DIGITAL BLOOD PRESSURE MONITOR, MODEL: KLOCK is DXQ.

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Other records listing Industrielle Entwicklung Medizintechnik Und Vertri 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.

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Related Devices (Code: DXQ)

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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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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