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FDA 510(k)

SEPTOCAL CAVITY LINER

K-Number: K913574 · 1991-09-30

Decision Date1991-09-30
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SEPTOCAL CAVITY LINER is the device name listed in this FDA 510(k) record. The listed applicant is Specialites Septodont. It received FDA 510(k) clearance on 1991-09-30 under 510(k) number K913574. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEPTOCAL CAVITY LINER?

SEPTOCAL CAVITY LINER is a medical device that received FDA 510(k) clearance on 1991-09-30. The listed applicant is Specialites Septodont. The 510(k) number is K913574.

When did SEPTOCAL CAVITY LINER receive FDA 510(k) clearance?

SEPTOCAL CAVITY LINER received FDA 510(k) clearance on 1991-09-30, under 510(k) number K913574.

Who is the listed applicant for SEPTOCAL CAVITY LINER?

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

What is the FDA product code for SEPTOCAL CAVITY LINER?

The FDA product code for SEPTOCAL CAVITY LINER is EJK.

Related Clinical Trials

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.

Other records listing Specialites Septodont as applicant

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.

View all 21 devices →

Related Devices (Code: EJK)

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.

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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