Devices

Device Recall Anspach eMax 2 Modified Hand Control

Model / Serial
Part Number: 98-0016; Serial Numbers: 200008201, 200008202, 200008203, 200008204, 200008205, 200008206.
Product Classification
Neurological Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution - USA including AL, CA, FL, IA, IL, KY, MN, MS, NC, OH, OK, PA, TN, TX.and Internationally to Canada, Japan, Hungary, Korea and Sweden. .
Product Description
ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx Only*** || This device is intended to be used with Anspach Systems
Manufacturer
The Anspach Effort, Inc.
1 Event
- Recall of Device Recall Anspach eMax 2 Modified Hand Control

Manufacturer

The Anspach Effort, Inc.

Manufacturer Address
The Anspach Effort, Inc., 4500 Riverside Drive, Palm Beach Gardens FL 33410-4235
Manufacturer Parent Company (2017)
Johnson & Johnson
Source
USFDA

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