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FDA 510(k)

EASYGUIDE

K-Number: K071599 · 2007-07-11

ApplicantKeystone Dental, Inc.
Decision Date2007-07-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

EASYGUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Keystone Dental, Inc.. It received FDA 510(k) clearance on 2007-07-11 under 510(k) number K071599. 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 EASYGUIDE?

EASYGUIDE is a medical device that received FDA 510(k) clearance on 2007-07-11. The listed applicant is Keystone Dental, Inc.. The 510(k) number is K071599.

When did EASYGUIDE receive FDA 510(k) clearance?

EASYGUIDE received FDA 510(k) clearance on 2007-07-11, under 510(k) number K071599.

Who is the listed applicant for EASYGUIDE?

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

What is the FDA product code for EASYGUIDE?

The FDA product code for EASYGUIDE is LLZ.

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Other records listing Keystone Dental, Inc. 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.

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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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