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E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961301
510(k) Type
Traditional
Applicant
DELPHI CONSULTING GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1996
Days to Decision
68 days
Submission Type
Statement

E-SCOPE ELECTRONIC STETHOSCOPE MODEL 718-7120

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K961301
510(k) Type
Traditional
Applicant
DELPHI CONSULTING GROUP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1996
Days to Decision
68 days
Submission Type
Statement