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FDA 510(k)

13-550,13-560 WESCOTT SCOSSORS (EYE)

K-Number: K851768 · 1985-06-20

ApplicantArtiberia
Decision Date1985-06-20
Product CodeHNF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

13-550,13-560 WESCOTT SCOSSORS (EYE) 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 K851768. The device is classified under product code HNF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 13-550,13-560 WESCOTT SCOSSORS (EYE)?

13-550,13-560 WESCOTT SCOSSORS (EYE) is a medical device that received FDA 510(k) clearance on 1985-06-20. The listed applicant is Artiberia. The 510(k) number is K851768.

When did 13-550,13-560 WESCOTT SCOSSORS (EYE) receive FDA 510(k) clearance?

13-550,13-560 WESCOTT SCOSSORS (EYE) received FDA 510(k) clearance on 1985-06-20, under 510(k) number K851768.

Who is the listed applicant for 13-550,13-560 WESCOTT SCOSSORS (EYE)?

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

What is the FDA product code for 13-550,13-560 WESCOTT SCOSSORS (EYE)?

The FDA product code for 13-550,13-560 WESCOTT SCOSSORS (EYE) is HNF.

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.

View all 79 devices →

Related Devices (Code: HNF)

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

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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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