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UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801241
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1980
Days to Decision
34 days

UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K801241
510(k) Type
Traditional
Applicant
ARCO MEDICAL PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/30/1980
Days to Decision
34 days