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MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862335
510(k) Type
Traditional
Applicant
U.S. MFG. & MANAGEMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/24/1986
Days to Decision
35 days

MODIFIED I.V. START, RE-START, PEDI AND GERI-KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K862335
510(k) Type
Traditional
Applicant
U.S. MFG. & MANAGEMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
7/24/1986
Days to Decision
35 days