LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660— 510(k) K070881
Substantially EquivalentSapimed S.P.A.
FDA 510(k) clearance K070881 for LEM HEMORRHOIDAL LIGATOR, MODELS A.5650, A.5660, Substantially Equivalent on 2007-09-26. Applicant: Sapimed S.P.A.. Device class: 2.
Clearance details
- Applicant
- Sapimed S.P.A.
- Product code
- Code FHN
- Device class
- Class 2
- Regulation
- 21 CFR 876.4400
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
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