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PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119, PM1-0142)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021864
510(k) Type
Traditional
Applicant
PRIMELINE MEDICAL PRODUCTS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/23/2002
Days to Decision
109 days
Submission Type
Statement

PRIMAGARD NONSTERILE FEMORAL ANGIOGRAPHY DRAPES (MODELS PM1-0136, PM1-0119, PM1-0142)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021864
510(k) Type
Traditional
Applicant
PRIMELINE MEDICAL PRODUCTS, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
9/23/2002
Days to Decision
109 days
Submission Type
Statement