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DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930286
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
6/22/1993
Days to Decision
152 days
Submission Type
Summary

DRI-VENDT/PROVENT/ACCUVENT ARTERIAL BLOOD GAS KITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K930286
510(k) Type
Traditional
Applicant
CONCORD/PORTEX
Country
United States
FDA Decision
Substantially Equivalent - Kit with Drugs
Decision Date
6/22/1993
Days to Decision
152 days
Submission Type
Summary