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TEST, DETECTION, ANTINUCLEAR ANTIBODIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760206
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1976
Days to Decision
25 days

TEST, DETECTION, ANTINUCLEAR ANTIBODIES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760206
510(k) Type
Traditional
Applicant
INTL. DIAGNOSTIC TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/3/1976
Days to Decision
25 days