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8MM QUANTUM PULSE/SUPRIMA II PULSE GENERATORS

Page Type
Cleared 510(K)
510(k) Number
K911122
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1991
Days to Decision
65 days

8MM QUANTUM PULSE/SUPRIMA II PULSE GENERATORS

Page Type
Cleared 510(K)
510(k) Number
K911122
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/16/1991
Days to Decision
65 days