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V*CARE MANUAL RESUSCITATOR, CAT#VR-1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913900
510(k) Type
Traditional
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1992
Days to Decision
130 days
Submission Type
Statement

V*CARE MANUAL RESUSCITATOR, CAT#VR-1000

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913900
510(k) Type
Traditional
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/7/1992
Days to Decision
130 days
Submission Type
Statement