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FDA 510(k)

A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR

K-Number: K002061 · 2001-01-19

ApplicantA&D Engineering, Inc.
Decision Date2001-01-19
Product CodeDRT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is A&D Engineering, Inc.. It received FDA 510(k) clearance on 2001-01-19 under 510(k) number K002061. The device is classified under product code DRT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR?

A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR is a medical device that received FDA 510(k) clearance on 2001-01-19. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K002061.

When did A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR receive FDA 510(k) clearance?

A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR received FDA 510(k) clearance on 2001-01-19, under 510(k) number K002061.

Who is the listed applicant for A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR?

The FDA 510(k) record lists A&D Engineering, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR?

The FDA product code for A&D MEDICAL TM-2550/TM-2551/TM-2560 VITAL SENSOR MONITOR is DRT.

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Related Devices (Code: DRT)

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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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