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FDA 510(k), K951228, ASH-7000
FDA 510(k), K951228, ASH-7000
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510(K) Number: K951228
Device Name: ASH-7000
Manufacturer: BRENDA CASSELL
Device Classification Name: Equipment, Traction, Powered
Regulation Number: ITH
Classification Product Code: KXA
Date Received: 03/20/1995
Decision Date: 05/17/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: ASH-7000
Manufacturer: BRENDA CASSELL
Device Classification Name: Equipment, Traction, Powered
Regulation Number: ITH
Classification Product Code: KXA
Date Received: 03/20/1995
Decision Date: 05/17/1995
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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