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MS 16 SYRINGE DRIVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802400
510(k) Type
Traditional
Applicant
PRINCETON MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1980
Days to Decision
75 days

MS 16 SYRINGE DRIVER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K802400
510(k) Type
Traditional
Applicant
PRINCETON MEDICAL INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/16/1980
Days to Decision
75 days