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ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800838
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
50 days

ARCOLITH 3022&ARCOLITH 3023 CARDIAC GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K800838
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1980
Days to Decision
50 days