REPROCESSED ENDOSCOPIC TROCAR— 510(k) K052299
Substantially EquivalentSterilmed, Inc.
FDA 510(k) clearance K052299 for REPROCESSED ENDOSCOPIC TROCAR, Substantially Equivalent on 2006-05-23. Applicant: Sterilmed, Inc.. Device class: 2.
Clearance details
- Applicant
- Sterilmed, Inc.
- Product code
- Code NLM
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- 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.