ANCHORAGE SCOPE, MODEL 000003— 510(k) K080780
Substantially EquivalentEpitek, Inc.
FDA 510(k) clearance K080780 for ANCHORAGE SCOPE, MODEL 000003, Substantially Equivalent on 2008-07-30. Applicant: Epitek, Inc.. Device class: 2.
Clearance details
- Applicant
- Epitek, Inc.
- Product code
- Code FBO
- Device class
- Class 2
- Regulation
- 21 CFR 876.1500
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bloomington, MN, US
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More clearances from Epitek, Inc.
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