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MODEL 230-05 CYBERLITH I BIPOL. PULSE G.

Page Type
Cleared 510(K)
510(k) Number
K810800
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1981
Days to Decision
39 days

MODEL 230-05 CYBERLITH I BIPOL. PULSE G.

Page Type
Cleared 510(K)
510(k) Number
K810800
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/1981
Days to Decision
39 days