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PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040)

Page Type
Cleared 510(K)
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)
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