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Master Caution Device MCD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142476
510(k) Type
Traditional
Applicant
HealthWatch Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/17/2015
Days to Decision
167 days
Submission Type
Summary

Master Caution Device MCD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142476
510(k) Type
Traditional
Applicant
HealthWatch Ltd.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
2/17/2015
Days to Decision
167 days
Submission Type
Summary