VENTRESCREEN (TM) MONO— 510(k) K872032
Substantially EquivalentVentrex Laboratories, Inc.
FDA 510(k) clearance K872032 for VENTRESCREEN (TM) MONO, Substantially Equivalent on 1987-06-29. Applicant: Ventrex Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Ventrex Laboratories, Inc.
- Product code
- Code KTN
- Device class
- Class 2
- Regulation
- 21 CFR 866.5640
- Advisory panel
- Immunology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Portland, ME, US
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