SUPRASORB A +AG— 510(k) K071442
Substantially EquivalentSpecialty Fibres and Materials, Ltd.
FDA 510(k) clearance K071442 for SUPRASORB A +AG, Substantially Equivalent on 2008-05-01. Applicant: Specialty Fibres and Materials, Ltd.. Device class: Unclassified.
Clearance details
- Applicant
- Specialty Fibres and Materials, Ltd.
- Product code
- Code FRO
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Coventry, GB
Recent devices under product code FRO
view allMore clearances from Specialty Fibres and Materials, Ltd.
view allAdverse 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 K071442
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 K071442.
Data sourced from openFDA. This site is unofficial and independent of the FDA.