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FDA 510(k)

INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003

K-Number: K071307 · 2008-02-12

ApplicantInviro Medical Devices, Inc.
Decision Date2008-02-12
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003 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 2008-02-12 under 510(k) number K071307. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003?

INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003 is a medical device that received FDA 510(k) clearance on 2008-02-12. The listed applicant is Inviro Medical Devices, Inc.. The 510(k) number is K071307.

When did INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003 receive FDA 510(k) clearance?

INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003 received FDA 510(k) clearance on 2008-02-12, under 510(k) number K071307.

Who is the listed applicant for INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003?

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 INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003?

The FDA product code for INVIROLINK AND INVIRO TIP BLUNT CANNULAS, MODEL 130001, 130501, 140001, 140002, 140003 is FMI.

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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.

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