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FDA 510(k)

MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717

K-Number: K896392 · 1989-11-28

ApplicantMedtronic Vascular
Decision Date1989-11-28
Product CodeCAZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1989-11-28 under 510(k) number K896392. 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 MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717?

MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717 is a medical device that received FDA 510(k) clearance on 1989-11-28. The listed applicant is Medtronic Vascular. The 510(k) number is K896392.

When did MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717 receive FDA 510(k) clearance?

MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717 received FDA 510(k) clearance on 1989-11-28, under 510(k) number K896392.

Who is the listed applicant for MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717?

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

What is the FDA product code for MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717?

The FDA product code for MEDTRONIC EPIDURAL CATHETER KIT MODEL 8717 is CAZ.

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Related Devices (Code: 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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