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ARCOLITH 4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791165
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1979
Days to Decision
15 days

ARCOLITH 4000

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K791165
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/10/1979
Days to Decision
15 days