Last synced on 25 January 2026 at 3:41 am

MODEL 230-05 CYBERLITH I BIPOL. PULSE G.

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
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