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FDA 510(k)

PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)

K-Number: K233777 · 2024-05-24

Decision Date2024-05-24
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) is a medical device manufactured by Primed Medical Products, Inc.. It received FDA 510(k) clearance on 2024-05-24 under approval number K233777. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)?

PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) is a medical device that received FDA 510(k) clearance on 2024-05-24. It is manufactured by Primed Medical Products, Inc.. The 510(k) number is K233777.

When was PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) approved by the FDA?

PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) received FDA 510(k) clearance on 2024-05-24, under approval number K233777.

What company makes PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)?

PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) is manufactured by Primed Medical Products, Inc..

What is the FDA product code for PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600)?

The FDA product code for PRIMED Sterilization Wrap (P100, P200, P300, P400, P500, P600) is FRG.

Other Devices by Primed Medical Products, Inc.

Related Devices (Code: FRG)

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.