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FDA 510(k)

LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT

K-Number: K970776 · 1997-05-27

ApplicantLifecore Biomedical, Inc.
Decision Date1997-05-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Lifecore Biomedical, Inc.. It received FDA 510(k) clearance on 1997-05-27 under 510(k) number K970776. 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 LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT?

LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT is a medical device that received FDA 510(k) clearance on 1997-05-27. The listed applicant is Lifecore Biomedical, Inc.. The 510(k) number is K970776.

When did LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT receive FDA 510(k) clearance?

LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT received FDA 510(k) clearance on 1997-05-27, under 510(k) number K970776.

Who is the listed applicant for LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT?

The FDA 510(k) record lists Lifecore Biomedical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT?

The FDA product code for LIFECORE O-RING ABUTMENT;LIFECORE DALLA BONA ABUTMENT is DZE.

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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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