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FDA 510(k)

RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A

K-Number: K060077 · 2006-03-08

ApplicantReal Tone Technology Corp.
Decision Date2006-03-08
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A is the device name listed in this FDA 510(k) record. The listed applicant is Real Tone Technology Corp.. It received FDA 510(k) clearance on 2006-03-08 under 510(k) number K060077. 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 RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A?

RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A is a medical device that received FDA 510(k) clearance on 2006-03-08. The listed applicant is Real Tone Technology Corp.. The 510(k) number is K060077.

When did RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A receive FDA 510(k) clearance?

RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A received FDA 510(k) clearance on 2006-03-08, under 510(k) number K060077.

Who is the listed applicant for RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A?

The FDA 510(k) record lists Real Tone Technology Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A?

The FDA product code for RTT DIGITAL WRIST BLOOD PRESSURE MONITOR, MODEL RTW-8010A 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.

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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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