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EMI MODEL FFF-IA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952164
510(k) Type
Traditional
Applicant
NEW YORK HEART INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1995
Days to Decision
7 days
Submission Type
Statement

EMI MODEL FFF-IA

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952164
510(k) Type
Traditional
Applicant
NEW YORK HEART INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/10/1995
Days to Decision
7 days
Submission Type
Statement