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CUSTOMED CYSTO PACK I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902274
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/20/1990
Days to Decision
122 days

CUSTOMED CYSTO PACK I

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902274
510(k) Type
Traditional
Applicant
CUSTOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
9/20/1990
Days to Decision
122 days