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FDA 510(k)

C0-AXIAL INTRODUCER NEEDLE

K-Number: K981721 · 1998-07-28

ApplicantInrad
Decision Date1998-07-28
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

C0-AXIAL INTRODUCER NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Inrad. It received FDA 510(k) clearance on 1998-07-28 under 510(k) number K981721. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C0-AXIAL INTRODUCER NEEDLE?

C0-AXIAL INTRODUCER NEEDLE is a medical device that received FDA 510(k) clearance on 1998-07-28. The listed applicant is Inrad. The 510(k) number is K981721.

When did C0-AXIAL INTRODUCER NEEDLE receive FDA 510(k) clearance?

C0-AXIAL INTRODUCER NEEDLE received FDA 510(k) clearance on 1998-07-28, under 510(k) number K981721.

Who is the listed applicant for C0-AXIAL INTRODUCER NEEDLE?

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

What is the FDA product code for C0-AXIAL INTRODUCER NEEDLE?

The FDA product code for C0-AXIAL INTRODUCER NEEDLE is KNW.

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Related Devices (Code: KNW)

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

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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