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FDA 510(k)

MODIFICATION TO KAVO QUATTROCARE

K-Number: K071288 · 2007-07-19

ApplicantSybron Dental Specialties, Inc.
Decision Date2007-07-19
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO KAVO QUATTROCARE is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Dental Specialties, Inc.. It received FDA 510(k) clearance on 2007-07-19 under 510(k) number K071288. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO KAVO QUATTROCARE?

MODIFICATION TO KAVO QUATTROCARE is a medical device that received FDA 510(k) clearance on 2007-07-19. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K071288.

When did MODIFICATION TO KAVO QUATTROCARE receive FDA 510(k) clearance?

MODIFICATION TO KAVO QUATTROCARE received FDA 510(k) clearance on 2007-07-19, under 510(k) number K071288.

Who is the listed applicant for MODIFICATION TO KAVO QUATTROCARE?

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

What is the FDA product code for MODIFICATION TO KAVO QUATTROCARE?

The FDA product code for MODIFICATION TO KAVO QUATTROCARE is EBF.

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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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