FDA 510(k)

INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022

K-Number: K083851 · 2009-05-15

Decision Date2009-05-15

Product CodeLHI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022 is the device name listed in this FDA 510(k) record. The listed applicant is Inviro Medical Devices, Inc.. It received FDA 510(k) clearance on 2009-05-15 under 510(k) number K083851. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022?

INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022 is a medical device that received FDA 510(k) clearance on 2009-05-15. The listed applicant is Inviro Medical Devices, Inc.. The 510(k) number is K083851.

When did INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022 receive FDA 510(k) clearance?

INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022 received FDA 510(k) clearance on 2009-05-15, under 510(k) number K083851.

Who is the listed applicant for INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022?

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

What is the FDA product code for INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022?

The FDA product code for INVIROBLUNT CANNULA WITH AND WITHOUT EZ WINGS, MODELS 120522 AND 120022 is LHI.

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Other records listing Inviro Medical Devices, Inc. as applicant

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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.