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FDA 510(k), K911296, OPTICAL CATHETER ARTHROSCOPE
FDA 510(k), K911296, OPTICAL CATHETER ARTHROSCOPE
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510(K) Number: K911296
Device Name: OPTICAL CATHETER ARTHROSCOPE
Manufacturer: MEDICAL DYNAMICS, INC.
Device Classification Name: arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 03/25/1991
Decision Date: 09/24/1991
Regulation Medical Specialty: Orthopedic
Device Name: OPTICAL CATHETER ARTHROSCOPE
Manufacturer: MEDICAL DYNAMICS, INC.
Device Classification Name: arthroscope
Regulation Number: 888.1100
Classification Product Code: HRX
Date Received: 03/25/1991
Decision Date: 09/24/1991
Regulation Medical Specialty: Orthopedic
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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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