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PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040178
510(k) Type
Traditional
Applicant
S.P.O. MEDICAL EQUIPMENT, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/10/2004
Days to Decision
228 days
Submission Type
Summary

PULSEOX 5500 FINGER DEVICE, PULSEOX 7500 WRISTWATCH DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K040178
510(k) Type
Traditional
Applicant
S.P.O. MEDICAL EQUIPMENT, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
9/10/2004
Days to Decision
228 days
Submission Type
Summary