VESSEL OCCLUDER— 510(k) K895726
Substantially EquivalentApplied Medical Technologies
FDA 510(k) clearance K895726 for VESSEL OCCLUDER, Substantially Equivalent on 1989-10-24. Applicant: Applied Medical Technologies. Device class: 1.
Clearance details
- Applicant
- Applied Medical Technologies
- Product code
- Code GDJ
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Independence, OH, US
Recent devices under product code GDJ
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Data sourced from openFDA. This site is unofficial and independent of the FDA.