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MOUTH TO FACE RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K873043
510(k) Type
Traditional
Applicant
ARTEC ENVIRONMENTAL MONITORING DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1987
Days to Decision
55 days

MOUTH TO FACE RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K873043
510(k) Type
Traditional
Applicant
ARTEC ENVIRONMENTAL MONITORING DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/1987
Days to Decision
55 days