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FDA 510(k)

WDS, SIZE 2 AND SIZE 2

K-Number: K061114 · 2006-06-06

ApplicantCefla S.C.R.L.
Decision Date2006-06-06
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

WDS, SIZE 2 AND SIZE 2 is the device name listed in this FDA 510(k) record. The listed applicant is Cefla S.C.R.L.. It received FDA 510(k) clearance on 2006-06-06 under 510(k) number K061114. 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 WDS, SIZE 2 AND SIZE 2?

WDS, SIZE 2 AND SIZE 2 is a medical device that received FDA 510(k) clearance on 2006-06-06. The listed applicant is Cefla S.C.R.L.. The 510(k) number is K061114.

When did WDS, SIZE 2 AND SIZE 2 receive FDA 510(k) clearance?

WDS, SIZE 2 AND SIZE 2 received FDA 510(k) clearance on 2006-06-06, under 510(k) number K061114.

Who is the listed applicant for WDS, SIZE 2 AND SIZE 2?

The FDA 510(k) record lists Cefla S.C.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WDS, SIZE 2 AND SIZE 2?

The FDA product code for WDS, SIZE 2 AND SIZE 2 is MUH.

Other records listing Cefla S.C.R.L. 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.

K080076RX DC X-RAY UNITK062897C-U2

Related Devices (Code: MUH)

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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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