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HOLTER RECORDER H3+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043010
510(k) Type
Abbreviated
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2005
Days to Decision
116 days
Submission Type
Summary

HOLTER RECORDER H3+

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K043010
510(k) Type
Abbreviated
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2005
Days to Decision
116 days
Submission Type
Summary