FDA 510(k)

ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER

K-Number: K092875 · 2010-08-13

Decision Date2010-08-13

Product CodeNBW

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2010-08-13 under 510(k) number K092875. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER?

ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER is a medical device that received FDA 510(k) clearance on 2010-08-13. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K092875.

When did ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER receive FDA 510(k) clearance?

ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER received FDA 510(k) clearance on 2010-08-13, under 510(k) number K092875.

Who is the listed applicant for ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER?

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

What is the FDA product code for ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER?

The FDA product code for ECHO TD-3227 DUAL BLOOD PRESSURE/BLOOD GLUCOSE METER is NBW. This falls under the OB/GYN category.

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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.