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FDA 510(k)

NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE

K-Number: K921886 · 1992-10-05

Decision Date1992-10-05
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Needle Technologies, Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K921886. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE?

NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Needle Technologies, Inc.. The 510(k) number is K921886.

When did NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE receive FDA 510(k) clearance?

NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE received FDA 510(k) clearance on 1992-10-05, under 510(k) number K921886.

Who is the listed applicant for NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE?

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

What is the FDA product code for NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE?

The FDA product code for NEEDLE TECHNOLOGIES SEED IMPLANT NEEDLE is IWJ.

Related Clinical Trials

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.

Related Devices (Code: IWJ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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