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PRO 2 MONITOR, PRO 2 SENSOR, PRO2 HOLDER, PRO2 NEONATE HOLDER, MODELS, PRO- 200, ANS-200, AHL-200, NHL-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032831
510(k) Type
Traditional
Applicant
CONMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2004
Days to Decision
355 days
Submission Type
Summary

PRO 2 MONITOR, PRO 2 SENSOR, PRO2 HOLDER, PRO2 NEONATE HOLDER, MODELS, PRO- 200, ANS-200, AHL-200, NHL-200

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032831
510(k) Type
Traditional
Applicant
CONMED CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2004
Days to Decision
355 days
Submission Type
Summary