ACTH RIA SYSTEM-DSI 2300— 510(k) K830893
Substantially EquivalentDiagnostic Systems Laboratories, Inc.
FDA 510(k) clearance K830893 for ACTH RIA SYSTEM-DSI 2300, Substantially Equivalent on 1983-04-27. Applicant: Diagnostic Systems Laboratories, Inc.. Device class: 2.
Clearance details
- Applicant
- Diagnostic Systems Laboratories, Inc.
- Product code
- Code CKG
- Device class
- Class 2
- Regulation
- 21 CFR 862.1025
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
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