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FDA 510(k)

Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology

K-Number: K151405 · 2016-01-26

Decision Date2016-01-26
Product CodeNLQ
DecisionSubstantially Equivalent

Device Summary

Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology is a medical device manufactured by Surgical Instrument Services and Savings(Dba Medline Renewal. It received FDA 510(k) clearance on 2016-01-26 under approval number K151405. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology?

Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology is a medical device that received FDA 510(k) clearance on 2016-01-26. It is manufactured by Surgical Instrument Services and Savings(Dba Medline Renewal. The 510(k) number is K151405.

When was Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology approved by the FDA?

Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology received FDA 510(k) clearance on 2016-01-26, under approval number K151405.

What company makes Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology?

Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology is manufactured by Surgical Instrument Services and Savings(Dba Medline Renewal.

What is the FDA product code for Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology?

The FDA product code for Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology is NLQ.

Related Clinical Trials

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Official Source

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