FDA 510(k)

EXPA-SYL

K-Number: K050180 · 2005-02-11

ApplicantProduits Dentaires Pierre Rolland

Decision Date2005-02-11

Product CodeMVL

DecisionSubstantially Equivalent

Device Summary

EXPA-SYL is the device name listed in this FDA 510(k) record. The listed applicant is Produits Dentaires Pierre Rolland. It received FDA 510(k) clearance on 2005-02-11 under 510(k) number K050180. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPA-SYL?

EXPA-SYL is a medical device that received FDA 510(k) clearance on 2005-02-11. The listed applicant is Produits Dentaires Pierre Rolland. The 510(k) number is K050180.

When did EXPA-SYL receive FDA 510(k) clearance?

EXPA-SYL received FDA 510(k) clearance on 2005-02-11, under 510(k) number K050180.

Who is the listed applicant for EXPA-SYL?

The FDA 510(k) record lists Produits Dentaires Pierre Rolland as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPA-SYL?

The FDA product code for EXPA-SYL is MVL.

Other records listing Produits Dentaires Pierre Rolland 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.

K111978SULCUS BLUE

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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.