Last synced on 14 November 2025 at 11:06 pm

2000 SERIES PORTABLE RESUSCITATION SYST.

Page Type
Cleared 510(K)
510(k) Number
K812519
510(k) Type
Traditional
Applicant
LIFE SCIENCE INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1981
Days to Decision
23 days

2000 SERIES PORTABLE RESUSCITATION SYST.

Page Type
Cleared 510(K)
510(k) Number
K812519
510(k) Type
Traditional
Applicant
LIFE SCIENCE INSTRUMENTATION, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/1981
Days to Decision
23 days