PROVIAL II #006-010-0201— 510(k) K823773
Substantially EquivalentDynatech Corp.
FDA 510(k) clearance K823773 for PROVIAL II #006-010-0201, Substantially Equivalent on 1983-01-21. Applicant: Dynatech Corp.. Device class: 1.
Clearance details
- Applicant
- Dynatech Corp.
- Product code
- Code KDT
- Device class
- Class 1
- Regulation
- 21 CFR 864.3250
- Advisory panel
- Pathology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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