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FDA 510(k), K092713, SPECTRE WIRELESS ENCRYPTED FOOTSWITCH AND HAND SWITCH SYSTEM
FDA 510(k), K092713, SPECTRE WIRELESS ENCRYPTED FOOTSWITCH AND HAND SWITCH SYSTEM
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510(K) Number: K092713
Device Name: SPECTRE WIRELESS ENCRYPTED FOOTSWITCH AND HAND SWITCH SYSTEM
Manufacturer: TRANSAMERICAN MEDICAL IMAGING
Device Classification Name: system, x-ray, mobile
Regulation Number: 892.1720
Classification Product Code: IZL
Date Received: 09/03/2009
Decision Date: 07/16/2010
Regulation Medical Specialty: Radiology
Device Name: SPECTRE WIRELESS ENCRYPTED FOOTSWITCH AND HAND SWITCH SYSTEM
Manufacturer: TRANSAMERICAN MEDICAL IMAGING
Device Classification Name: system, x-ray, mobile
Regulation Number: 892.1720
Classification Product Code: IZL
Date Received: 09/03/2009
Decision Date: 07/16/2010
Regulation Medical Specialty: Radiology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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