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ADULT VENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K834352
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1984
Days to Decision
45 days

ADULT VENT CATHETER

Page Type
Cleared 510(K)
510(k) Number
K834352
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1984
Days to Decision
45 days