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FDA 510(k)

41-180 TO 41-246 VARIOUS NASAL FORCEPS

K-Number: K851794 · 1985-06-11

ApplicantArtiberia
Decision Date1985-06-11
Product CodeKAE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

41-180 TO 41-246 VARIOUS NASAL FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Artiberia. It received FDA 510(k) clearance on 1985-06-11 under 510(k) number K851794. The device is classified under product code KAE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 41-180 TO 41-246 VARIOUS NASAL FORCEPS?

41-180 TO 41-246 VARIOUS NASAL FORCEPS is a medical device that received FDA 510(k) clearance on 1985-06-11. The listed applicant is Artiberia. The 510(k) number is K851794.

When did 41-180 TO 41-246 VARIOUS NASAL FORCEPS receive FDA 510(k) clearance?

41-180 TO 41-246 VARIOUS NASAL FORCEPS received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851794.

Who is the listed applicant for 41-180 TO 41-246 VARIOUS NASAL FORCEPS?

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 41-180 TO 41-246 VARIOUS NASAL FORCEPS?

The FDA product code for 41-180 TO 41-246 VARIOUS NASAL FORCEPS is KAE.

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: KAE)

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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