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SERAGAN ACTH125 I-RIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822115
510(k) Type
Traditional
Applicant
SERAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1982
Days to Decision
91 days

SERAGAN ACTH125 I-RIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822115
510(k) Type
Traditional
Applicant
SERAGEN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/18/1982
Days to Decision
91 days