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PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881616
510(k) Type
Traditional
Applicant
PROGRESS MANKIND TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1988
Days to Decision
150 days

PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K881616
510(k) Type
Traditional
Applicant
PROGRESS MANKIND TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1988
Days to Decision
150 days