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FDA 510(k)

13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT

K-Number: K851764 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product Code
DecisionSubstantially Equivalent

Device Summary

13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-20 under 510(k) number K851764. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT?

13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851764.

When did 13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT receive FDA 510(k) clearance?

13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851764.

Who is the listed applicant for 13-340,13-350,13-360 LIGATURE SCISSORE SPENCER/LIT?

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

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 Artiberia 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.

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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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