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SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952518
510(k) Type
Traditional
Applicant
MEDI-DOSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1995
Days to Decision
102 days
Submission Type
Statement

SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952518
510(k) Type
Traditional
Applicant
MEDI-DOSE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/1995
Days to Decision
102 days
Submission Type
Statement