Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K081257 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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ACT Cellular Phone Monitor; a component of the ACT Ambulatory Cardiac Telemetry; an automatically ac... | 2 | 11/17/2011 | Lifewatch Services Inc |
LifeStar ACT III Platinum Sensor Ambulatory Cardiac Telemetry; an automatically activated system wit... | 2 | 11/17/2011 | Lifewatch Services Inc |
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