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MODIFICATION TO WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILLUMINOMETRIC (ICMA) ASSAY KIT, MODEL 3KG002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060420
510(k) Type
Special
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2006
Days to Decision
12 days
Submission Type
Statement

MODIFICATION TO WHOLE PTH (1-84) SPECIFIC IMMUNOCHEMILLUMINOMETRIC (ICMA) ASSAY KIT, MODEL 3KG002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060420
510(k) Type
Special
Applicant
SCANTIBODIES LABORATORY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2006
Days to Decision
12 days
Submission Type
Statement