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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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