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CORDIS STIMUCORD EXTERNAL NEUTRAL STIM

Page Type
Cleared 510(K)
510(k) Number
K810319
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1981
Days to Decision
13 days

CORDIS STIMUCORD EXTERNAL NEUTRAL STIM

Page Type
Cleared 510(K)
510(k) Number
K810319
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/19/1981
Days to Decision
13 days