Last synced on 30 September 2022 at 11:05 pm

PIONEER PRO-PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914220
510(k) Type
Traditional
Applicant
PIONEER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
167 days
Submission Type
Statement

PIONEER PRO-PUMP

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914220
510(k) Type
Traditional
Applicant
PIONEER MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1992
Days to Decision
167 days
Submission Type
Statement