Last synced on 14 November 2025 at 11:06 pm

1ST RESPONSE REUSABLE MANUAL RESUSCITATOR (ADULT)

Page Type
Cleared 510(K)
510(k) Number
K900577
510(k) Type
Traditional
Applicant
INTERTECH RESOURCES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1990
Days to Decision
159 days

1ST RESPONSE REUSABLE MANUAL RESUSCITATOR (ADULT)

Page Type
Cleared 510(K)
510(k) Number
K900577
510(k) Type
Traditional
Applicant
INTERTECH RESOURCES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/16/1990
Days to Decision
159 days