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IV START KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914475
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
3/18/1992
Days to Decision
162 days
Submission Type
Statement

IV START KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914475
510(k) Type
Traditional
Applicant
CYPRESS MEDICAL PRODUCTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
3/18/1992
Days to Decision
162 days
Submission Type
Statement