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EIDOS 5003 HOLTER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952969
510(k) Type
Traditional
Applicant
New Product Development, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1996
Days to Decision
385 days
Submission Type
Statement

EIDOS 5003 HOLTER SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952969
510(k) Type
Traditional
Applicant
New Product Development, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1996
Days to Decision
385 days
Submission Type
Statement