REPROCESSED HARMONIC SCALPELS— 510(k) K050343
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K050343 for REPROCESSED HARMONIC SCALPELS, Substantially Equivalent on 2005-04-12. 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
- Maple Grove, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.