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FDA 510(k)

EPINEED EPIDURAL NEEDLE

K-Number: K832233 · 1983-08-08

ApplicantTerumo Medical Corp.
Decision Date1983-08-08
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EPINEED EPIDURAL NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Terumo Medical Corp.. It received FDA 510(k) clearance on 1983-08-08 under 510(k) number K832233. 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 EPINEED EPIDURAL NEEDLE?

EPINEED EPIDURAL NEEDLE is a medical device that received FDA 510(k) clearance on 1983-08-08. The listed applicant is Terumo Medical Corp.. The 510(k) number is K832233.

When did EPINEED EPIDURAL NEEDLE receive FDA 510(k) clearance?

EPINEED EPIDURAL NEEDLE received FDA 510(k) clearance on 1983-08-08, under 510(k) number K832233.

Who is the listed applicant for EPINEED EPIDURAL NEEDLE?

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

What is the FDA product code for EPINEED EPIDURAL NEEDLE?

The FDA product code for EPINEED EPIDURAL NEEDLE is BSP.

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Other records listing Terumo Medical Corp. as applicant

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Related Devices (Code: BSP)

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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.

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