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FDA 510(k)

SWISSMEDA DENTAL PLANNING SYSTEM

K-Number: K112251 · 2012-01-25

ApplicantSwissmeda AG
Decision Date2012-01-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SWISSMEDA DENTAL PLANNING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Swissmeda AG. It received FDA 510(k) clearance on 2012-01-25 under 510(k) number K112251. 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 SWISSMEDA DENTAL PLANNING SYSTEM?

SWISSMEDA DENTAL PLANNING SYSTEM is a medical device that received FDA 510(k) clearance on 2012-01-25. The listed applicant is Swissmeda AG. The 510(k) number is K112251.

When did SWISSMEDA DENTAL PLANNING SYSTEM receive FDA 510(k) clearance?

SWISSMEDA DENTAL PLANNING SYSTEM received FDA 510(k) clearance on 2012-01-25, under 510(k) number K112251.

Who is the listed applicant for SWISSMEDA DENTAL PLANNING SYSTEM?

The FDA 510(k) record lists Swissmeda AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SWISSMEDA DENTAL PLANNING SYSTEM?

The FDA product code for SWISSMEDA DENTAL PLANNING SYSTEM is LLZ.

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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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