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)

BYRON NASAL SEPTAL BUTTON

K-Number: K863398 · 1986-09-17

ApplicantByron Medical
Decision Date1986-09-17
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BYRON NASAL SEPTAL BUTTON is the device name listed in this FDA 510(k) record. The listed applicant is Byron Medical. It received FDA 510(k) clearance on 1986-09-17 under 510(k) number K863398. The device is classified under product code FZE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BYRON NASAL SEPTAL BUTTON?

BYRON NASAL SEPTAL BUTTON is a medical device that received FDA 510(k) clearance on 1986-09-17. The listed applicant is Byron Medical. The 510(k) number is K863398.

When did BYRON NASAL SEPTAL BUTTON receive FDA 510(k) clearance?

BYRON NASAL SEPTAL BUTTON received FDA 510(k) clearance on 1986-09-17, under 510(k) number K863398.

Who is the listed applicant for BYRON NASAL SEPTAL BUTTON?

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

What is the FDA product code for BYRON NASAL SEPTAL BUTTON?

The FDA product code for BYRON NASAL SEPTAL BUTTON is FZE.

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 Byron Medical 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 27 devices →

Related Devices (Code: FZE)

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.

↑