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MYOGLOBIN RIA TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915233
510(k) Type
Traditional
Applicant
PRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1992
Days to Decision
129 days
Submission Type
Statement

MYOGLOBIN RIA TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K915233
510(k) Type
Traditional
Applicant
PRO DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/30/1992
Days to Decision
129 days
Submission Type
Statement