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MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913714
510(k) Type
Traditional
Applicant
LIFE DESIGN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1992
Days to Decision
474 days
Submission Type
Statement

MODIFICATION MANUAL PULMON RESUSCITOR/PULMANEX(TM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913714
510(k) Type
Traditional
Applicant
LIFE DESIGN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1992
Days to Decision
474 days
Submission Type
Statement