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FDA 510(k)

GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB

K-Number: K952275 · 1995-10-11

ApplicantGlobal Medical Prods, Inc.
Decision Date1995-10-11
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Prods, Inc.. It received FDA 510(k) clearance on 1995-10-11 under 510(k) number K952275. 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 GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB?

GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB is a medical device that received FDA 510(k) clearance on 1995-10-11. The listed applicant is Global Medical Prods, Inc.. The 510(k) number is K952275.

When did GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB receive FDA 510(k) clearance?

GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB received FDA 510(k) clearance on 1995-10-11, under 510(k) number K952275.

Who is the listed applicant for GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB?

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

What is the FDA product code for GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB?

The FDA product code for GLOBAL MEDICAL PRODUCTS TUOHY & CRAWFORD EPIDURAL NEEDLE W/PLASTIC HUB is 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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