Last synced on 14 November 2025 at 11:06 pm

PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-1

Page Type
Cleared 510(K)
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)
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