TRI-PLEX ADAPTER— 510(k) K010401
Substantially EquivalentThe Medical Device Group, Inc.
FDA 510(k) clearance K010401 for TRI-PLEX ADAPTER, Substantially Equivalent on 2002-10-30. Applicant: The Medical Device Group, Inc.. Device class: 2.
Clearance details
- Applicant
- The Medical Device Group, Inc.
- Product code
- Code MOD
- Device class
- Class 2
- Regulation
- 21 CFR 868.5895
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Crofton, MD, US
Recent devices under product code MOD
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