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THEREX R-PORT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932671
510(k) Type
Traditional
Applicant
THEREX CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/7/1994
Days to Decision
250 days
Submission Type
Statement

THEREX R-PORT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K932671
510(k) Type
Traditional
Applicant
THEREX CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
2/7/1994
Days to Decision
250 days
Submission Type
Statement