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)

DR. JAPAN FACIL POINT SPINAL NEEDLE

K-Number: K020934 · 2002-10-25

ApplicantMyco Medical, Inc.
Decision Date2002-10-25
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DR. JAPAN FACIL POINT SPINAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical, Inc.. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K020934. 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 DR. JAPAN FACIL POINT SPINAL NEEDLE?

DR. JAPAN FACIL POINT SPINAL NEEDLE is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Myco Medical, Inc.. The 510(k) number is K020934.

When did DR. JAPAN FACIL POINT SPINAL NEEDLE receive FDA 510(k) clearance?

DR. JAPAN FACIL POINT SPINAL NEEDLE received FDA 510(k) clearance on 2002-10-25, under 510(k) number K020934.

Who is the listed applicant for DR. JAPAN FACIL POINT SPINAL NEEDLE?

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

What is the FDA product code for DR. JAPAN FACIL POINT SPINAL NEEDLE?

The FDA product code for DR. JAPAN FACIL POINT SPINAL NEEDLE 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

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.

↑