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FDA 510(k)

BIONIC-TOOTH-PLANT MODEL A-1

K-Number: K873437 · 1988-06-13

ApplicantLarry R. Ashkinazy, D.D.S.
Decision Date1988-06-13
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BIONIC-TOOTH-PLANT MODEL A-1 is the device name listed in this FDA 510(k) record. The listed applicant is Larry R. Ashkinazy, D.D.S.. It received FDA 510(k) clearance on 1988-06-13 under 510(k) number K873437. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIONIC-TOOTH-PLANT MODEL A-1?

BIONIC-TOOTH-PLANT MODEL A-1 is a medical device that received FDA 510(k) clearance on 1988-06-13. The listed applicant is Larry R. Ashkinazy, D.D.S.. The 510(k) number is K873437.

When did BIONIC-TOOTH-PLANT MODEL A-1 receive FDA 510(k) clearance?

BIONIC-TOOTH-PLANT MODEL A-1 received FDA 510(k) clearance on 1988-06-13, under 510(k) number K873437.

Who is the listed applicant for BIONIC-TOOTH-PLANT MODEL A-1?

The FDA 510(k) record lists Larry R. Ashkinazy, D.D.S. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BIONIC-TOOTH-PLANT MODEL A-1?

The FDA product code for BIONIC-TOOTH-PLANT MODEL A-1 is DZE.

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Related Devices (Code: DZE)

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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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