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FDA 510(k)

QuikClot Control+

K-Number: K200167 · 2020-04-23

ApplicantZ-Medica, LLC
Decision Date2020-04-23
Product CodePOD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

QuikClot Control+ is a medical device manufactured by Z-Medica, LLC. It received FDA 510(k) clearance on 2020-04-23 under approval number K200167. The device is classified under product code POD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QuikClot Control+?

QuikClot Control+ is a medical device that received FDA 510(k) clearance on 2020-04-23. It is manufactured by Z-Medica, LLC. The 510(k) number is K200167.

When was QuikClot Control+ approved by the FDA?

QuikClot Control+ received FDA 510(k) clearance on 2020-04-23, under approval number K200167.

What company makes QuikClot Control+?

QuikClot Control+ is manufactured by Z-Medica, LLC.

What is the FDA product code for QuikClot Control+?

The FDA product code for QuikClot Control+ is POD.

Other Devices by Z-Medica, LLC

DEN160012D2 Dressing K181641QuikClot Radial K220971QuikClot Control+ Hemostatic Dressing

Related Devices (Code: POD)

DEN160012D2 DressingZ-Medica, LLC K183190NuStatBeeken Biomedical, LLC K220971QuikClot Control+ Hemostatic DressingZ-Medica, LLC K213198Ax-Surgi Surgical HemostatAdvamedica, Inc. K243553QuikClot Control+ Hemostatic DeviceTeleflex Medical

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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