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FDA 510(k)

STINGRAY EPIDURAL CATHETER CONNECTOR

K-Number: K051171 · 2005-08-26

ApplicantEpimed International, Inc.
Decision Date2005-08-26
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STINGRAY EPIDURAL CATHETER CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Epimed International, Inc.. It received FDA 510(k) clearance on 2005-08-26 under 510(k) number K051171. The device is classified under product code CAZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STINGRAY EPIDURAL CATHETER CONNECTOR?

STINGRAY EPIDURAL CATHETER CONNECTOR is a medical device that received FDA 510(k) clearance on 2005-08-26. The listed applicant is Epimed International, Inc.. The 510(k) number is K051171.

When did STINGRAY EPIDURAL CATHETER CONNECTOR receive FDA 510(k) clearance?

STINGRAY EPIDURAL CATHETER CONNECTOR received FDA 510(k) clearance on 2005-08-26, under 510(k) number K051171.

Who is the listed applicant for STINGRAY EPIDURAL CATHETER CONNECTOR?

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

What is the FDA product code for STINGRAY EPIDURAL CATHETER CONNECTOR?

The FDA product code for STINGRAY EPIDURAL CATHETER CONNECTOR is CAZ.

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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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