MEDLINE COLLAGEN WOUND DRESSING— 510(k) K060456
Substantially EquivalentMedline Industries, Inc.
FDA 510(k) clearance K060456 for MEDLINE COLLAGEN WOUND DRESSING, Substantially Equivalent on 2006-06-19. Applicant: Medline Industries, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Medline Industries, Inc.
- Product code
- Code KGN
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Mundelein, IL, US
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Adverse events under product code KGN
product code KGN- Other
- 2
- Total
- 2
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recalls naming K060456
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K060456.
Data sourced from openFDA. This site is unofficial and independent of the FDA.