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FDA 510(k)

PERIO PROTECT TRAY

K-Number: K031809 · 2004-01-23

ApplicantPerio Protect, LLC
Decision Date2004-01-23
Product CodeKMT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIO PROTECT TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Perio Protect, LLC. It received FDA 510(k) clearance on 2004-01-23 under 510(k) number K031809. The device is classified under product code KMT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIO PROTECT TRAY?

PERIO PROTECT TRAY is a medical device that received FDA 510(k) clearance on 2004-01-23. The listed applicant is Perio Protect, LLC. The 510(k) number is K031809.

When did PERIO PROTECT TRAY receive FDA 510(k) clearance?

PERIO PROTECT TRAY received FDA 510(k) clearance on 2004-01-23, under 510(k) number K031809.

Who is the listed applicant for PERIO PROTECT TRAY?

The FDA 510(k) record lists Perio Protect, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERIO PROTECT TRAY?

The FDA product code for PERIO PROTECT TRAY is KMT.

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Related Devices (Code: KMT)

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.

K904914DENTAL VACUUM INJECTION TRAYThe Lebanon Vac-Tray Corp.K871784TOP FORM II TRAYS, DISPOS FOAM-LINED TOP GEL APPLIColgate-Hoyt LaboratoriesK853882SUPER SLICKTang ProductsK820104NUPRO* GEL TRAYJohnson & Johnson Professionals, Inc.K811154HOYT ECONO-TRAYHoyt LaboratoriesK780712KERR DISCOVERY DISPOSABLE FLUORIDE TRAYKerr Corporation (Danbury)

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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