Last synced on 14 November 2025 at 11:06 pm

CARDIOBEEPER(R) III

Page Type
Cleared 510(K)
510(k) Number
K880300
510(k) Type
Traditional
Applicant
SURVIVAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1988
Days to Decision
108 days

CARDIOBEEPER(R) III

Page Type
Cleared 510(K)
510(k) Number
K880300
510(k) Type
Traditional
Applicant
SURVIVAL TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/12/1988
Days to Decision
108 days