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FDA 510(k)

POINT 4 MODIFIED

K-Number: K013510 · 2002-01-18

ApplicantSybron Dental Specialties, Inc.
Decision Date2002-01-18
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

POINT 4 MODIFIED 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 2002-01-18 under 510(k) number K013510. 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 POINT 4 MODIFIED?

POINT 4 MODIFIED is a medical device that received FDA 510(k) clearance on 2002-01-18. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K013510.

When did POINT 4 MODIFIED receive FDA 510(k) clearance?

POINT 4 MODIFIED received FDA 510(k) clearance on 2002-01-18, under 510(k) number K013510.

Who is the listed applicant for POINT 4 MODIFIED?

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 POINT 4 MODIFIED?

The FDA product code for POINT 4 MODIFIED 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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