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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 35 Results
510(K) Number: K080802
 
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Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Electronic Foot Control with Direction Switch Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
eMax2 PLUS Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Console, eMax2 Plus Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
System Console, Single Port, with irrigation Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Reciprocating MICRO SAW 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
20.2cm Heavy Duty Long Heavy Short Attachment 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Sagittal MICRO-SAW 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Sagittal Saw Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
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