SPARK-KIT(TM)— 510(k) K864509
Substantially EquivalentLyphomed, Inc.
FDA 510(k) clearance K864509 for SPARK-KIT(TM), Substantially Equivalent on 1987-02-18. Applicant: Lyphomed, Inc..
Clearance details
- Applicant
- Lyphomed, Inc.
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Melrose Park, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.