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SORIN PULSE GENERATOR MODEL # LIT 214 H

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792565
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1980
Days to Decision
60 days

SORIN PULSE GENERATOR MODEL # LIT 214 H

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K792565
510(k) Type
Traditional
Applicant
BENTLEY LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1980
Days to Decision
60 days