Last synced on 14 November 2025 at 11:06 pm

INDEFLATOR

Page Type
Cleared 510(K)
510(k) Number
K813622
510(k) Type
Traditional
Applicant
ADVANCED CATHETER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
24 days

INDEFLATOR

Page Type
Cleared 510(K)
510(k) Number
K813622
510(k) Type
Traditional
Applicant
ADVANCED CATHETER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1982
Days to Decision
24 days