ACTH RIA— 510(k) K833849
Substantially EquivalentSyncor Intl. Corp.
FDA 510(k) clearance K833849 for ACTH RIA, Substantially Equivalent on 1984-01-30. Applicant: Syncor Intl. Corp.. Device class: 2.
Clearance details
- Applicant
- Syncor Intl. Corp.
- 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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More clearances from Syncor Intl. Corp.
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