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)

MEDIZIV SPINAL NEEDLE SET

K-Number: K925831 · 1993-07-16

ApplicantMedicia Medical Products
Decision Date1993-07-16
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIZIV SPINAL NEEDLE SET is the device name listed in this FDA 510(k) record. The listed applicant is Medicia Medical Products. It received FDA 510(k) clearance on 1993-07-16 under 510(k) number K925831. 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 MEDIZIV SPINAL NEEDLE SET?

MEDIZIV SPINAL NEEDLE SET is a medical device that received FDA 510(k) clearance on 1993-07-16. The listed applicant is Medicia Medical Products. The 510(k) number is K925831.

When did MEDIZIV SPINAL NEEDLE SET receive FDA 510(k) clearance?

MEDIZIV SPINAL NEEDLE SET received FDA 510(k) clearance on 1993-07-16, under 510(k) number K925831.

Who is the listed applicant for MEDIZIV SPINAL NEEDLE SET?

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

What is the FDA product code for MEDIZIV SPINAL NEEDLE SET?

The FDA product code for MEDIZIV SPINAL NEEDLE SET 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 Medicia Medical Products 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.

K911128MEDIZIV INFUSION SET

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.

↑