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FDA 510(k)

FILMLESS CLINIC

K-Number: K031704 · 2003-07-31

ApplicantConnect Imaging, Inc.
Decision Date2003-07-31
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

FILMLESS CLINIC is the device name listed in this FDA 510(k) record. The listed applicant is Connect Imaging, Inc.. It received FDA 510(k) clearance on 2003-07-31 under 510(k) number K031704. 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 FILMLESS CLINIC?

FILMLESS CLINIC is a medical device that received FDA 510(k) clearance on 2003-07-31. The listed applicant is Connect Imaging, Inc.. The 510(k) number is K031704.

When did FILMLESS CLINIC receive FDA 510(k) clearance?

FILMLESS CLINIC received FDA 510(k) clearance on 2003-07-31, under 510(k) number K031704.

Who is the listed applicant for FILMLESS CLINIC?

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

What is the FDA product code for FILMLESS CLINIC?

The FDA product code for FILMLESS CLINIC is LLZ.

Related Clinical Trials

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Other records listing Connect Imaging, 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.

K061972CONNECT IMAGING PACS

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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.

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