Last synced on 14 November 2025 at 11:06 pm

UNIPOLAR PROGRAMMABLE LITHIUM CARD. GEN.

Page Type
Cleared 510(K)
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)
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