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FDA 510(k)

LIFESOURCE MODELS UA-787, UA 787PC, UA-787T

K-Number: K012013 · 2001-07-13

ApplicantA&D Engineering, Inc.
Decision Date2001-07-13
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFESOURCE MODELS UA-787, UA 787PC, UA-787T 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 2001-07-13 under 510(k) number K012013. 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 LIFESOURCE MODELS UA-787, UA 787PC, UA-787T?

LIFESOURCE MODELS UA-787, UA 787PC, UA-787T is a medical device that received FDA 510(k) clearance on 2001-07-13. The listed applicant is A&D Engineering, Inc.. The 510(k) number is K012013.

When did LIFESOURCE MODELS UA-787, UA 787PC, UA-787T receive FDA 510(k) clearance?

LIFESOURCE MODELS UA-787, UA 787PC, UA-787T received FDA 510(k) clearance on 2001-07-13, under 510(k) number K012013.

Who is the listed applicant for LIFESOURCE MODELS UA-787, UA 787PC, UA-787T?

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 LIFESOURCE MODELS UA-787, UA 787PC, UA-787T?

The FDA product code for LIFESOURCE MODELS UA-787, UA 787PC, UA-787T is DXN.

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Related Devices (Code: DXN)

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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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