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FDA 510(k)

CTC WORKSTATION, MODEL 2200

K-Number: K062229 · 2006-09-11

ApplicantMedical Diagnostic Technologies, Inc.
Decision Date2006-09-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CTC WORKSTATION, MODEL 2200 is the device name listed in this FDA 510(k) record. The listed applicant is Medical Diagnostic Technologies, Inc.. It received FDA 510(k) clearance on 2006-09-11 under 510(k) number K062229. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CTC WORKSTATION, MODEL 2200?

CTC WORKSTATION, MODEL 2200 is a medical device that received FDA 510(k) clearance on 2006-09-11. The listed applicant is Medical Diagnostic Technologies, Inc.. The 510(k) number is K062229.

When did CTC WORKSTATION, MODEL 2200 receive FDA 510(k) clearance?

CTC WORKSTATION, MODEL 2200 received FDA 510(k) clearance on 2006-09-11, under 510(k) number K062229.

Who is the listed applicant for CTC WORKSTATION, MODEL 2200?

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

What is the FDA product code for CTC WORKSTATION, MODEL 2200?

The FDA product code for CTC WORKSTATION, MODEL 2200 is LLZ.

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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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