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NO-POKES NEEDLE SAFETY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020921
510(k) Type
Traditional
Applicant
BEMIS MFG. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2002
Days to Decision
112 days
Submission Type
Statement

NO-POKES NEEDLE SAFETY DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020921
510(k) Type
Traditional
Applicant
BEMIS MFG. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/11/2002
Days to Decision
112 days
Submission Type
Statement