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FDA 510(k)

TCAL ABUTMENT

K-Number: K913782 · 1991-10-30

ApplicantCore-Vent Corp.
Decision Date1991-10-30
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TCAL ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Core-Vent Corp.. It received FDA 510(k) clearance on 1991-10-30 under 510(k) number K913782. 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 TCAL ABUTMENT?

TCAL ABUTMENT is a medical device that received FDA 510(k) clearance on 1991-10-30. The listed applicant is Core-Vent Corp.. The 510(k) number is K913782.

When did TCAL ABUTMENT receive FDA 510(k) clearance?

TCAL ABUTMENT received FDA 510(k) clearance on 1991-10-30, under 510(k) number K913782.

Who is the listed applicant for TCAL ABUTMENT?

The FDA 510(k) record lists Core-Vent Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TCAL ABUTMENT?

The FDA product code for TCAL ABUTMENT is DZE.

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Other records listing Core-Vent Corp. as applicant

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Related Devices (Code: DZE)

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

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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