JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT— 510(k) K925467

Unknown

J.J. Skinner, Inc.

FDA 510(k) clearance K925467 for JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT, Unknown on 1994-05-11. Applicant: J.J. Skinner, Inc..

Clearance details

Applicant: J.J. Skinner, Inc.
Product code: Code LRO
Advisory panel: General, Plastic Surgery
Date received: 1992-10-29
Decision date: 1994-05-11
Decision: Unknown
Clearance type: Traditional
Location: Great Neck, NY, US

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Adverse events under product code LRO

product code LRO

Injury: 975
Malfunction: 14,038
Other: 2
Total: 15,015

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.