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FDA 510(k)

E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY

K-Number: K933711 · 1993-11-22

ApplicantNeurodelivery Technology, Inc.
Decision Date1993-11-22
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Neurodelivery Technology, Inc.. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K933711. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY?

E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is Neurodelivery Technology, Inc.. The 510(k) number is K933711.

When did E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY receive FDA 510(k) clearance?

E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY received FDA 510(k) clearance on 1993-11-22, under 510(k) number K933711.

Who is the listed applicant for E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY?

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

What is the FDA product code for E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY?

The FDA product code for E-SP COMBINED EPIDURAL-SPINAL ANESTHESIA TRAY is CAZ.

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Other records listing Neurodelivery Technology, 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.

K933721EPIDURAL ANESTHESIA PROCEDURE TRAY, CUSTOMK934526MICRO-SP CUSTOM SPINAL ANESTHESIA TRAY

Related Devices (Code: CAZ)

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.

K261372Profoject™ LOR SyringeCMT Health PTE., Ltd.K222341Arrow 0.2 Micron Flat Filter, GVSArrow International, LLCK210983BD Epilor SyringeBecton, Dickinson and CompanyK201356Plastic LOR SyringeJiangsu Caina Medical Co.,LtdK202699E-Cath STIM acc. TsuiPAJUNK GmbH MedizintechnologieK190345VPCPAJUNK 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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