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FDA 510(k)

SONICFILL 2010

K-Number: K091091 · 2009-10-14

ApplicantSybron Dental Specialties, Inc.
Decision Date2009-10-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SONICFILL 2010 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 2009-10-14 under 510(k) number K091091. 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 SONICFILL 2010?

SONICFILL 2010 is a medical device that received FDA 510(k) clearance on 2009-10-14. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K091091.

When did SONICFILL 2010 receive FDA 510(k) clearance?

SONICFILL 2010 received FDA 510(k) clearance on 2009-10-14, under 510(k) number K091091.

Who is the listed applicant for SONICFILL 2010?

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 SONICFILL 2010?

The FDA product code for SONICFILL 2010 is EBF.

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Other records listing Sybron Dental Specialties, Inc. as applicant

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Related Devices (Code: 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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