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FDA 510(k)

CS 7600

K-Number: K111649 · 2011-09-23

ApplicantCarestream Health, Inc.
Decision Date2011-09-23
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CS 7600 is the device name listed in this FDA 510(k) record. The listed applicant is Carestream Health, Inc.. It received FDA 510(k) clearance on 2011-09-23 under 510(k) number K111649. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CS 7600?

CS 7600 is a medical device that received FDA 510(k) clearance on 2011-09-23. The listed applicant is Carestream Health, Inc.. The 510(k) number is K111649.

When did CS 7600 receive FDA 510(k) clearance?

CS 7600 received FDA 510(k) clearance on 2011-09-23, under 510(k) number K111649.

Who is the listed applicant for CS 7600?

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

What is the FDA product code for CS 7600?

The FDA product code for CS 7600 is MUH.

Other records listing Carestream Health, Inc. as applicant

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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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