Medihoney Wound Gel— 510(k) K150985
Substantially EquivalentDerma Sciences, Inc.
FDA 510(k) clearance K150985 for Medihoney Wound Gel, Substantially Equivalent on 2015-11-19. Applicant: Derma Sciences, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Derma Sciences, Inc.
- Product code
- Code FRO
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Toronto, Orntario, CA
Recent devices under product code FRO
view allMore clearances from Derma Sciences, Inc.
view all- K133279 — MEDIHONEY WOUND DRESSINGS
- K110546 — MEDIHONEY HYDROGEL SHEET DRESSINGS WITH ACTIVE LEPTOSPERMUM HONEY
- K101793 — MEDIHONEY GEL DRESSING WITH ACTIVE MANUKA HONEY
- K081584 — DERMA SCIENCES OTC MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY
- K080315 — DERMA SCIENCES MEDIHONEY DRESSINGS WITH ACTIVE MANUKA HONEY
Adverse events under product code FRO
product code FRO- Death
- 30
- Injury
- 653
- Malfunction
- 479
- Other
- 11
- Total
- 1,173
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 K150985
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 K150985.
Data sourced from openFDA. This site is unofficial and independent of the FDA.