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FDA 510(k)

INDENTEC DRILL RA #1

K-Number: K884187 · 1988-12-22

ApplicantPhillip C. Crawford, D.D.S.
Decision Date1988-12-22
Product CodeDZA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INDENTEC DRILL RA #1 is the device name listed in this FDA 510(k) record. The listed applicant is Phillip C. Crawford, D.D.S.. It received FDA 510(k) clearance on 1988-12-22 under 510(k) number K884187. The device is classified under product code DZA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INDENTEC DRILL RA #1?

INDENTEC DRILL RA #1 is a medical device that received FDA 510(k) clearance on 1988-12-22. The listed applicant is Phillip C. Crawford, D.D.S.. The 510(k) number is K884187.

When did INDENTEC DRILL RA #1 receive FDA 510(k) clearance?

INDENTEC DRILL RA #1 received FDA 510(k) clearance on 1988-12-22, under 510(k) number K884187.

Who is the listed applicant for INDENTEC DRILL RA #1?

The FDA 510(k) record lists Phillip C. Crawford, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INDENTEC DRILL RA #1?

The FDA product code for INDENTEC DRILL RA #1 is DZA.

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Related Devices (Code: DZA)

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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