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RESPOND II...NEUROMUSCULAR STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K813008
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
36 days

RESPOND II...NEUROMUSCULAR STIMULATOR

Page Type
Cleared 510(K)
510(k) Number
K813008
510(k) Type
Traditional
Applicant
MEDTRONIC VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1981
Days to Decision
36 days