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FDA 510(k)

MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE

K-Number: K901810 · 1991-05-30

ApplicantNeuro Technology
Decision Date1991-05-30
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Technology. It received FDA 510(k) clearance on 1991-05-30 under 510(k) number K901810. 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 MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE?

MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE is a medical device that received FDA 510(k) clearance on 1991-05-30. The listed applicant is Neuro Technology. The 510(k) number is K901810.

When did MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE receive FDA 510(k) clearance?

MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE received FDA 510(k) clearance on 1991-05-30, under 510(k) number K901810.

Who is the listed applicant for MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE?

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

What is the FDA product code for MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE?

The FDA product code for MICRO-SP LUMBAR PUNCTURE (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

Other records listing Neuro Technology 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.

K925014E-SP COMBINED EPI SPINAL MINISETK901811ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLEK822139STIMPENK822138NEUROSTIM II

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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