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SIMS 1ST RESPONSE MANUAL RESUSCITATOR, ADULT

Page Type
Cleared 510(K)
510(k) Number
K972283
510(k) Type
Traditional
Applicant
SIMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1997
Days to Decision
90 days
Submission Type
Statement

SIMS 1ST RESPONSE MANUAL RESUSCITATOR, ADULT

Page Type
Cleared 510(K)
510(k) Number
K972283
510(k) Type
Traditional
Applicant
SIMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/17/1997
Days to Decision
90 days
Submission Type
Statement