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PM-8 HEART RATE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864748
510(k) Type
Traditional
Applicant
PULSE TIME PRODUCTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/20/1987
Days to Decision
105 days

PM-8 HEART RATE MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864748
510(k) Type
Traditional
Applicant
PULSE TIME PRODUCTS, LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/20/1987
Days to Decision
105 days