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FDA 510(k)

KERR COMPOMER

K-Number: K974105 · 1998-01-09

ApplicantSybron Dental Specialties, Inc.
Decision Date1998-01-09
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

KERR COMPOMER 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 1998-01-09 under 510(k) number K974105. 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 KERR COMPOMER?

KERR COMPOMER is a medical device that received FDA 510(k) clearance on 1998-01-09. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K974105.

When did KERR COMPOMER receive FDA 510(k) clearance?

KERR COMPOMER received FDA 510(k) clearance on 1998-01-09, under 510(k) number K974105.

Who is the listed applicant for KERR COMPOMER?

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 KERR COMPOMER?

The FDA product code for KERR COMPOMER is EBF.

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Other records listing Sybron Dental Specialties, 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.

K093341CENTURY MODEL 105CK091091SONICFILL 2010K080089SONICFLEX 2003 AND SONICFLEX LUX 2003 L WITH INSTRUMENT TIPSK073478SUPERTORQUE HIGH-SPEED HANDPIECES AND GENTLEPOWER HANDPIECES AND ATTACHEMENTSK071615FIXAFLOSSK071288MODIFICATION TO KAVO QUATTROCARE

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Related Devices (Code: EBF)

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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