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MAXCESS NEEDLE FREE CONNECTOR (8200)

Page Type
Cleared 510(K)
510(k) Number
K960661
510(k) Type
Traditional
Applicant
SOLOPAK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1996
Days to Decision
34 days
Submission Type
Summary

MAXCESS NEEDLE FREE CONNECTOR (8200)

Page Type
Cleared 510(K)
510(k) Number
K960661
510(k) Type
Traditional
Applicant
SOLOPAK MEDICAL PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/1996
Days to Decision
34 days
Submission Type
Summary