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NELLCOR SYMPHONY N-3000 PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952316
510(k) Type
Traditional
Applicant
NELLCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1995
Days to Decision
92 days
Submission Type
Summary

NELLCOR SYMPHONY N-3000 PULSE OXIMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K952316
510(k) Type
Traditional
Applicant
NELLCOR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/1995
Days to Decision
92 days
Submission Type
Summary