Last synced on 14 November 2025 at 11:06 pm

ATRIUM 2050 CHEST DRAIN BLOOD RECOVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K897126
510(k) Type
Traditional
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1990
Days to Decision
77 days

ATRIUM 2050 CHEST DRAIN BLOOD RECOVERY SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K897126
510(k) Type
Traditional
Applicant
ATRIUM MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1990
Days to Decision
77 days