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PULMONARY RESUSCITATOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892221
510(k) Type
Traditional
Applicant
LIFE DESIGN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1989
Days to Decision
49 days

PULMONARY RESUSCITATOR, MODIFICATION

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K892221
510(k) Type
Traditional
Applicant
LIFE DESIGN SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/1989
Days to Decision
49 days