Last synced on 1 July 2022 at 11:04 pm

P.E.E.P. VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882219
510(k) Type
Traditional
Applicant
LIFE SUPPORT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1988
Days to Decision
96 days

P.E.E.P. VALVE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882219
510(k) Type
Traditional
Applicant
LIFE SUPPORT PRODUCTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/30/1988
Days to Decision
96 days