PermeaDerm B, PermeaDerm CW, and PermeaDerm Glove— 510(k) K153678

Name: FDA 510(k) clearance K153678
Creator: U.S. Food and Drug Administration
Published: 2016-08-08

Substantially Equivalent

Permeaderm, Inc.

FDA 510(k) clearance K153678 for PermeaDerm B, PermeaDerm CW, and PermeaDerm Glove, Substantially Equivalent on 2016-08-08. Applicant: Permeaderm, Inc.. Device class: Unclassified.

Clearance details

Applicant: Permeaderm, Inc.
Product code: Code FRO
Device class: Unclassified
Advisory panel: Unknown
Date received: 2015-12-21
Decision date: 2016-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carlsbad, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FRO

product code FRO

Death: 30
Injury: 653
Malfunction: 479
Other: 11
Total: 1,173

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.