FDA 510(k)

VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES

K-Number: K020113 · 2002-05-17

Decision Date2002-05-17

Product CodeEBF

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES is the device name listed in this FDA 510(k) record. The listed applicant is Vector Research & Development. It received FDA 510(k) clearance on 2002-05-17 under 510(k) number K020113. 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 VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES?

VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES is a medical device that received FDA 510(k) clearance on 2002-05-17. The listed applicant is Vector Research & Development. The 510(k) number is K020113.

When did VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES receive FDA 510(k) clearance?

VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES received FDA 510(k) clearance on 2002-05-17, under 510(k) number K020113.

Who is the listed applicant for VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES?

The FDA 510(k) record lists Vector Research & Development as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES?

The FDA product code for VECTOR F SERIES HIGH-SPEED DENTAL HANDPIECES is EBF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.