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FDA 510(k)

ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079

K-Number: K091300 · 2009-07-23

ApplicantCAO Group, Inc.
Decision Date2009-07-23
Product CodeKLE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 is the device name listed in this FDA 510(k) record. The listed applicant is CAO Group, Inc.. It received FDA 510(k) clearance on 2009-07-23 under 510(k) number K091300. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079?

ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 is a medical device that received FDA 510(k) clearance on 2009-07-23. The listed applicant is CAO Group, Inc.. The 510(k) number is K091300.

When did ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 receive FDA 510(k) clearance?

ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 received FDA 510(k) clearance on 2009-07-23, under 510(k) number K091300.

Who is the listed applicant for ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079?

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

What is the FDA product code for ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079?

The FDA product code for ASCENT PORCELAIN PRIMER, MODEL 006-00078, 00600079 is KLE.

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Related Devices (Code: KLE)

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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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