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V*CARE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012842
510(k) Type
Special
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2001
Days to Decision
26 days
Submission Type
Statement

V*CARE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012842
510(k) Type
Special
Applicant
VENTLAB CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2001
Days to Decision
26 days
Submission Type
Statement