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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K223822

ACTIVBRAID™ · Embody, Inc. · decided 2023-06-02 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
ActivBraidAB-150T-0BEmbody, Inc.GAT00810063820657
ACTIVBRAIDAB-200R-1WEmbody, Inc.GAT00810063820404
ActivBraidAB-200R-2WEmbody, Inc.GAT00810063820619
ACTIVBRAIDAB-021R-1BEmbody, Inc.GAT00810063820381
ActivBraidAB-150T-2WEmbody, Inc.GAT00810063820640
ACTIVBRAIDAB-250T-0WEmbody, Inc.GAT00810063820398
ActivBraidAB-150T-0WEmbody, Inc.GAT00810063820633
ACTIVBRAIDAB-150T-1BEmbody, Inc.GAT00810063820435
ACTIVBRAIDAB-200R-1BEmbody, Inc.GAT00810063820411
ActivBraidAB-200R-2BEmbody, Inc.GAT00810063820626
ACTIVBRAIDAB-250T-0BEmbody, Inc.GAT00810063820442
ActivBraidAB-150T-2BEmbody, Inc.GAT00810063820664
ACTIVBRAIDAB-150T-1WEmbody, Inc.GAT00810063820428
ActivBraidAB-021R-2BEmbody, Inc.GAT00810063820602