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FDA 510(k)

MEDLOG, MODEL 1-0-10

K-Number: K060756 · 2006-10-30

ApplicantBmc Gesellschaft Fur Medizintechnik Mbh
Decision Date2006-10-30
Product CodeMWI
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDLOG, MODEL 1-0-10 is the device name listed in this FDA 510(k) record. The listed applicant is Bmc Gesellschaft Fur Medizintechnik Mbh. It received FDA 510(k) clearance on 2006-10-30 under 510(k) number K060756. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLOG, MODEL 1-0-10?

MEDLOG, MODEL 1-0-10 is a medical device that received FDA 510(k) clearance on 2006-10-30. The listed applicant is Bmc Gesellschaft Fur Medizintechnik Mbh. The 510(k) number is K060756.

When did MEDLOG, MODEL 1-0-10 receive FDA 510(k) clearance?

MEDLOG, MODEL 1-0-10 received FDA 510(k) clearance on 2006-10-30, under 510(k) number K060756.

Who is the listed applicant for MEDLOG, MODEL 1-0-10?

The FDA 510(k) record lists Bmc Gesellschaft Fur Medizintechnik Mbh as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDLOG, MODEL 1-0-10?

The FDA product code for MEDLOG, MODEL 1-0-10 is MWI.

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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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