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)

FLOWERS NASAL IMPLANT

K-Number: K904656 · 1990-12-18

Decision Date1990-12-18
Product CodeFZE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLOWERS NASAL IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Implantech Associates, Inc.. It received FDA 510(k) clearance on 1990-12-18 under 510(k) number K904656. 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 FLOWERS NASAL IMPLANT?

FLOWERS NASAL IMPLANT is a medical device that received FDA 510(k) clearance on 1990-12-18. The listed applicant is Implantech Associates, Inc.. The 510(k) number is K904656.

When did FLOWERS NASAL IMPLANT receive FDA 510(k) clearance?

FLOWERS NASAL IMPLANT received FDA 510(k) clearance on 1990-12-18, under 510(k) number K904656.

Who is the listed applicant for FLOWERS NASAL IMPLANT?

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

What is the FDA product code for FLOWERS NASAL IMPLANT?

The FDA product code for FLOWERS NASAL IMPLANT 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 Implantech Associates, Inc. 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 40 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.

↑