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FDA 510(k)

IN6 SAFETY SYRINGE, MODEL 3ML

K-Number: K051800 · 2005-10-21

Decision Date2005-10-21
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IN6 SAFETY SYRINGE, MODEL 3ML is the device name listed in this FDA 510(k) record. The listed applicant is In6 Incuvestor, Inc.. It received FDA 510(k) clearance on 2005-10-21 under 510(k) number K051800. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN6 SAFETY SYRINGE, MODEL 3ML?

IN6 SAFETY SYRINGE, MODEL 3ML is a medical device that received FDA 510(k) clearance on 2005-10-21. The listed applicant is In6 Incuvestor, Inc.. The 510(k) number is K051800.

When did IN6 SAFETY SYRINGE, MODEL 3ML receive FDA 510(k) clearance?

IN6 SAFETY SYRINGE, MODEL 3ML received FDA 510(k) clearance on 2005-10-21, under 510(k) number K051800.

Who is the listed applicant for IN6 SAFETY SYRINGE, MODEL 3ML?

The FDA 510(k) record lists In6 Incuvestor, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN6 SAFETY SYRINGE, MODEL 3ML?

The FDA product code for IN6 SAFETY SYRINGE, MODEL 3ML is MEG.

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: MEG)

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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