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FDA 510(k)

GENYX MEDICAL INJECTION NEEDLE

K-Number: K990996 · 1999-06-18

Decision Date1999-06-18
Product CodeFBK
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GENYX MEDICAL INJECTION NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Genyx Medical, Inc.. It received FDA 510(k) clearance on 1999-06-18 under 510(k) number K990996. The device is classified under product code FBK. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENYX MEDICAL INJECTION NEEDLE?

GENYX MEDICAL INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 1999-06-18. The listed applicant is Genyx Medical, Inc.. The 510(k) number is K990996.

When did GENYX MEDICAL INJECTION NEEDLE receive FDA 510(k) clearance?

GENYX MEDICAL INJECTION NEEDLE received FDA 510(k) clearance on 1999-06-18, under 510(k) number K990996.

Who is the listed applicant for GENYX MEDICAL INJECTION NEEDLE?

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

What is the FDA product code for GENYX MEDICAL INJECTION NEEDLE?

The FDA product code for GENYX MEDICAL INJECTION NEEDLE is FBK.

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: FBK)

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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