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FDA 510(k)

DENTAL PREP WASH AND PREP DISINFECT

K-Number: K962909 · 1996-10-07

ApplicantWilliam J. Day
Decision Date1996-10-07
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL PREP WASH AND PREP DISINFECT is the device name listed in this FDA 510(k) record. The listed applicant is William J. Day. It received FDA 510(k) clearance on 1996-10-07 under 510(k) number K962909. 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 DENTAL PREP WASH AND PREP DISINFECT?

DENTAL PREP WASH AND PREP DISINFECT is a medical device that received FDA 510(k) clearance on 1996-10-07. The listed applicant is William J. Day. The 510(k) number is K962909.

When did DENTAL PREP WASH AND PREP DISINFECT receive FDA 510(k) clearance?

DENTAL PREP WASH AND PREP DISINFECT received FDA 510(k) clearance on 1996-10-07, under 510(k) number K962909.

Who is the listed applicant for DENTAL PREP WASH AND PREP DISINFECT?

The FDA 510(k) record lists William J. Day as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DENTAL PREP WASH AND PREP DISINFECT?

The FDA product code for DENTAL PREP WASH AND PREP DISINFECT is EBF.

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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

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

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