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)

PHOENIX EPIDURAL & SPINAL NEEDLES

K-Number: K990519 · 2000-06-02

ApplicantMyco Medical Supplies, Inc.
Decision Date2000-06-02
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PHOENIX EPIDURAL & SPINAL NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 2000-06-02 under 510(k) number K990519. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHOENIX EPIDURAL & SPINAL NEEDLES?

PHOENIX EPIDURAL & SPINAL NEEDLES is a medical device that received FDA 510(k) clearance on 2000-06-02. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K990519.

When did PHOENIX EPIDURAL & SPINAL NEEDLES receive FDA 510(k) clearance?

PHOENIX EPIDURAL & SPINAL NEEDLES received FDA 510(k) clearance on 2000-06-02, under 510(k) number K990519.

Who is the listed applicant for PHOENIX EPIDURAL & SPINAL NEEDLES?

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

What is the FDA product code for PHOENIX EPIDURAL & SPINAL NEEDLES?

The FDA product code for PHOENIX EPIDURAL & SPINAL NEEDLES is BSP.

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 Myco Medical Supplies, 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.

K203668RELI NRFit Epidural Needles, Phoenix NRFit Epidural Needles, RELI NRFit Spinal Needles, Phoenix NRFit Spinal NeedlesK173279RELI Safety Blood Collection Tube Holder, RELI Blood Collection Tube HolderK090426VAKU-8 BLOOD COLLECTION NEEDLESK042504CATHY STERILE DISPOSABLE I.V. CANNULA WITH CATHETERK000592UNOLOK PLUS INFUSION SET AND VAKU-8 PLUS BLOOD COLLECTION SETK982646AILEE SUTURES AND AILEE NEEDLES

View all 12 devices →

Related Devices (Code: BSP)

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.

K243690SonoMSKPAJUNK GmbH MedizintechnologieK243682SonoPlex STIM; SonoPlex IIPAJUNK GmbH MedizintechnologieK250774SPROTTE® STANDARD (LUER/ NRFit®) Lumbar PuncturePAJUNK GmbH MedizintechnologieK243525SonoTAP and SonoTAP IIPAJUNK GmbH MedizintechnologieK241953SPROTTE® STANDARD (LUER/ NRFit®) AnesthesiologyPAJUNK GmbH MedizintechnologieK241954SonoBlock; SonoBlock IIPAJUNK GmbH Medizintechnologie

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.

↑