FDA 510(k)

ABBOTT ARCHITECT TOTAL T3

K-Number: K983434 · 1998-11-20

Decision Date1998-11-20

Product CodeCDP

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

ABBOTT ARCHITECT TOTAL T3 is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1998-11-20 under 510(k) number K983434. The device is classified under product code CDP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABBOTT ARCHITECT TOTAL T3?

ABBOTT ARCHITECT TOTAL T3 is a medical device that received FDA 510(k) clearance on 1998-11-20. The listed applicant is Abbott Laboratories. The 510(k) number is K983434.

When did ABBOTT ARCHITECT TOTAL T3 receive FDA 510(k) clearance?

ABBOTT ARCHITECT TOTAL T3 received FDA 510(k) clearance on 1998-11-20, under 510(k) number K983434.

Who is the listed applicant for ABBOTT ARCHITECT TOTAL T3?

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

What is the FDA product code for ABBOTT ARCHITECT TOTAL T3?

The FDA product code for ABBOTT ARCHITECT TOTAL T3 is CDP.

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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.