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FDA 510(k)

DSM Biomedical Porcine Pericardium Dental Membrane

K-Number: K160474 · 2016-06-07

ApplicantKensey Nash Corporation Dba Dsm Biomedical
Decision Date2016-06-07
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DSM Biomedical Porcine Pericardium Dental Membrane is a medical device manufactured by Kensey Nash Corporation Dba Dsm Biomedical. It received FDA 510(k) clearance on 2016-06-07 under approval number K160474. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSM Biomedical Porcine Pericardium Dental Membrane?

DSM Biomedical Porcine Pericardium Dental Membrane is a medical device that received FDA 510(k) clearance on 2016-06-07. It is manufactured by Kensey Nash Corporation Dba Dsm Biomedical. The 510(k) number is K160474.

When was DSM Biomedical Porcine Pericardium Dental Membrane approved by the FDA?

DSM Biomedical Porcine Pericardium Dental Membrane received FDA 510(k) clearance on 2016-06-07, under approval number K160474.

What company makes DSM Biomedical Porcine Pericardium Dental Membrane?

DSM Biomedical Porcine Pericardium Dental Membrane is manufactured by Kensey Nash Corporation Dba Dsm Biomedical.

What is the FDA product code for DSM Biomedical Porcine Pericardium Dental Membrane?

The FDA product code for DSM Biomedical Porcine Pericardium Dental Membrane is NPL.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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