Last synced on 14 November 2025 at 11:06 pm

BIPOLAR, STANICOR LAMBDA MODEL 236,235

Page Type
Cleared 510(K)
510(k) Number
K790014
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
36 days

BIPOLAR, STANICOR LAMBDA MODEL 236,235

Page Type
Cleared 510(K)
510(k) Number
K790014
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/8/1979
Days to Decision
36 days