Cleared Traditional

K212521 - Field Shield Wound Dressing (FDA 510(k) Clearance)

Jul 2024
Decision
1073d
Days
-
Risk

K212521 is an FDA 510(k) clearance for the Field Shield Wound Dressing. This device is classified as a Dressing, Wound, Drug.

Submitted by Kericure, Inc. (Wesley Chapel, US). The FDA issued a Cleared decision on July 18, 2024, 1073 days after receiving the submission on August 10, 2021.

This device falls under the General & Plastic Surgery FDA review panel.

Submission Details

510(k) Number K212521 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 10, 2021
Decision Date July 18, 2024
Days to Decision 1073 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code FRO - Dressing, Wound, Drug
Device Class -

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