FDA 510(k) Applications Submitted by SURVIVALINK CORP.

FDA 510(k) Number Submission Date Device Name Applicant
K011901 06/18/2001 FIRSTSAVE STAR BIPHASIC, MODEL 9210/9200 SURVIVALINK CORP.
K010214 01/23/2001 FIRSTSAVE BIPHASIC MODEL #9200 AND 9210 SURVIVALINK CORP.
K982264 06/29/1998 FIRSTSAVE BIPHASIC MODELS 9200 AND 9210 SURVIVALINK CORP.
K993072 09/14/1999 SURVIVALINK MULTIFUNCTIONAL ELECTRODE (SVL-9630) SURVIVALINK CORP.
K970481 02/10/1997 V2 SURVIVALINK CORP.
K971149 03/28/1997 SVL-9130 DEFIBRILLATION ELECTRODE SURVIVALINK CORP.


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