Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology— 510(k) K190610
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K190610 for Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology, Substantially Equivalent on 2019-08-15. Applicant: Sterilmed, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Sterilmed, Inc.
- Product code
- Code NLQ
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.