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FDA 510(k)

RP CUTTING NEEDLE

K-Number: K092059 · 2009-09-24

ApplicantRiverpoint Medical
Decision Date2009-09-24
Product CodeKNW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

RP CUTTING NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Riverpoint Medical. It received FDA 510(k) clearance on 2009-09-24 under 510(k) number K092059. 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 RP CUTTING NEEDLE?

RP CUTTING NEEDLE is a medical device that received FDA 510(k) clearance on 2009-09-24. The listed applicant is Riverpoint Medical. The 510(k) number is K092059.

When did RP CUTTING NEEDLE receive FDA 510(k) clearance?

RP CUTTING NEEDLE received FDA 510(k) clearance on 2009-09-24, under 510(k) number K092059.

Who is the listed applicant for RP CUTTING NEEDLE?

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

What is the FDA product code for RP CUTTING NEEDLE?

The FDA product code for RP CUTTING NEEDLE is KNW.

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Other records listing Riverpoint Medical as applicant

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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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