FLOSCOPE MICRODOP— 510(k) K910441
Substantially EquivalentAdvance Medical Device, Inc.
FDA 510(k) clearance K910441 for FLOSCOPE MICRODOP, Substantially Equivalent on 1991-03-21. Applicant: Advance Medical Device, Inc.. Device class: 2.
Clearance details
- Applicant
- Advance Medical Device, Inc.
- Product code
- Code DPT
- Device class
- Class 2
- Regulation
- 21 CFR 870.2120
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Berlin, NJ, US
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