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PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990960
510(k) Type
Traditional
Applicant
PERIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
185 days
Submission Type
Summary

PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K990960
510(k) Type
Traditional
Applicant
PERIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1999
Days to Decision
185 days
Submission Type
Summary