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HY-TEC/MANUAL AUTOIMMUNE KIT FOR HISTONE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962450
510(k) Type
Traditional
Applicant
Hycor Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
160 days
Submission Type
Statement

HY-TEC/MANUAL AUTOIMMUNE KIT FOR HISTONE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962450
510(k) Type
Traditional
Applicant
Hycor Biomedical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
160 days
Submission Type
Statement