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FDA 510(k)

E-SP COMBINED EPI SPINAL MINISET

K-Number: K925014 · 1993-04-19

ApplicantNeuro Technology
Decision Date1993-04-19
Product CodeCAZ
Advisory CommitteeAN
DecisionUnknown

Device Summary

E-SP COMBINED EPI SPINAL MINISET is the device name listed in this FDA 510(k) record. The listed applicant is Neuro Technology. It received FDA 510(k) clearance on 1993-04-19 under 510(k) number K925014. 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 EPI SPINAL MINISET?

E-SP COMBINED EPI SPINAL MINISET is a medical device that received FDA 510(k) clearance on 1993-04-19. The listed applicant is Neuro Technology. The 510(k) number is K925014.

When did E-SP COMBINED EPI SPINAL MINISET receive FDA 510(k) clearance?

E-SP COMBINED EPI SPINAL MINISET received FDA 510(k) clearance on 1993-04-19, under 510(k) number K925014.

Who is the listed applicant for E-SP COMBINED EPI SPINAL MINISET?

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 E-SP COMBINED EPI SPINAL MINISET?

The FDA product code for E-SP COMBINED EPI SPINAL MINISET is CAZ.

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Other records listing Neuro Technology as applicant

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K901810MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLEK901811ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLEK822139STIMPENK822138NEUROSTIM II

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.

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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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