Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS

K-Number: K851795 · 1985-06-11

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

Device Summary

41-250 TO 41-282 VARIOUS NASAL CUTTING 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 K851795. 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 41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS?

41-250 TO 41-282 VARIOUS NASAL CUTTING 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 K851795.

When did 41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS receive FDA 510(k) clearance?

41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS received FDA 510(k) clearance on 1985-06-11, under 510(k) number K851795.

Who is the listed applicant for 41-250 TO 41-282 VARIOUS NASAL CUTTING 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 41-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPS?

The FDA product code for 41-250 TO 41-282 VARIOUS NASAL CUTTING 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.

↑