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THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K827748
510(k) Type
Traditional
Applicant
KEMBLE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
27 days

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K827748
510(k) Type
Traditional
Applicant
KEMBLE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/1982
Days to Decision
27 days