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FDA 510(k)

DPILOG, MODEL DPC-512

K-Number: K062811 · 2006-12-20

ApplicantLife Outcomes, Inc.
Decision Date2006-12-20
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DPILOG, MODEL DPC-512 is the device name listed in this FDA 510(k) record. The listed applicant is Life Outcomes, Inc.. It received FDA 510(k) clearance on 2006-12-20 under 510(k) number K062811. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DPILOG, MODEL DPC-512?

DPILOG, MODEL DPC-512 is a medical device that received FDA 510(k) clearance on 2006-12-20. The listed applicant is Life Outcomes, Inc.. The 510(k) number is K062811.

When did DPILOG, MODEL DPC-512 receive FDA 510(k) clearance?

DPILOG, MODEL DPC-512 received FDA 510(k) clearance on 2006-12-20, under 510(k) number K062811.

Who is the listed applicant for DPILOG, MODEL DPC-512?

The FDA 510(k) record lists Life Outcomes, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DPILOG, MODEL DPC-512?

The FDA product code for DPILOG, MODEL DPC-512 is CAF.

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Official Source

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