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)

FLORET NASAL TAMPON

K-Number: K830263 · 1983-03-24

ApplicantRitmed, Inc.
Decision Date1983-03-24
Product CodeLYA
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FLORET NASAL TAMPON is the device name listed in this FDA 510(k) record. The listed applicant is Ritmed, Inc.. It received FDA 510(k) clearance on 1983-03-24 under 510(k) number K830263. The device is classified under product code LYA. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLORET NASAL TAMPON?

FLORET NASAL TAMPON is a medical device that received FDA 510(k) clearance on 1983-03-24. The listed applicant is Ritmed, Inc.. The 510(k) number is K830263.

When did FLORET NASAL TAMPON receive FDA 510(k) clearance?

FLORET NASAL TAMPON received FDA 510(k) clearance on 1983-03-24, under 510(k) number K830263.

Who is the listed applicant for FLORET NASAL TAMPON?

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

What is the FDA product code for FLORET NASAL TAMPON?

The FDA product code for FLORET NASAL TAMPON is LYA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Ritmed, 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.

K833626FLORET FOAM PREP SPONGEK832874ISOVIS WOUND PROTECTORK830270ISOVIS WOUND PROTECTORK830261FLORET STRUNG GAUZE SPONGESK830268FLORET CYLINDRICAL/BRONCHOSCOPIC/LAMINK830266FLORET KITTNER OR K DISSECTOR

View all 22 devices →

Related Devices (Code: LYA)

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.

K243655TurbAlignSpirair, Inc.K230142Epi-Stop Nasal Gel/epistaxis packBiomed Ent, Inc.K213153SPIWay Endonasal Access GuideSpiway, LLCK202623Novapak Nasal Sinus Packing and StentMedtronic XomedK181696ChitoZolveGyrus Acmi, Inc.K180141SPIWay Endonasal Access GuideSpiway, LLC

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.

↑