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ZEE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K812022
510(k) Type
Traditional
Applicant
ZEE MEDICAL PRODUCTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1981
Days to Decision
11 days

ZEE MANUAL RESUSCITATOR

Page Type
Cleared 510(K)
510(k) Number
K812022
510(k) Type
Traditional
Applicant
ZEE MEDICAL PRODUCTS CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/1981
Days to Decision
11 days