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FDA 510(k)

MDILOG, MODEL MDC-512

K-Number: K990185 · 1999-04-01

ApplicantMedtrak Technologies, Inc.
Decision Date1999-04-01
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MDILOG, MODEL MDC-512 is the device name listed in this FDA 510(k) record. The listed applicant is Medtrak Technologies, Inc.. It received FDA 510(k) clearance on 1999-04-01 under 510(k) number K990185. 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 MDILOG, MODEL MDC-512?

MDILOG, MODEL MDC-512 is a medical device that received FDA 510(k) clearance on 1999-04-01. The listed applicant is Medtrak Technologies, Inc.. The 510(k) number is K990185.

When did MDILOG, MODEL MDC-512 receive FDA 510(k) clearance?

MDILOG, MODEL MDC-512 received FDA 510(k) clearance on 1999-04-01, under 510(k) number K990185.

Who is the listed applicant for MDILOG, MODEL MDC-512?

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

What is the FDA product code for MDILOG, MODEL MDC-512?

The FDA product code for MDILOG, MODEL MDC-512 is CAF.

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Other records listing Medtrak Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K970344MDILOG, MODEL MDC-511

Related Devices (Code: CAF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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