REPROCESSED GUIDEWIRES— 510(k) K012556
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K012556 for REPROCESSED GUIDEWIRES, Substantially Equivalent on 2002-04-29. Applicant: Sterilmed, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterilmed, Inc.
- Product code
- Code NML
- Device class
- Class 2
- Regulation
- 21 CFR 876.5010
- Advisory panel
- Gastroenterology, Urology
- 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.