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FDA 510(k), K962611, BARD EAGLE INFLATION DEVICE
FDA 510(k), K962611, BARD EAGLE INFLATION DEVICE
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510(K) Number: K962611
Device Name: BARD EAGLE INFLATION DEVICE
Manufacturer: RYDER INTL. CORP.
Device Classification Name: dilator, urethral
Regulation Number: 876.5520
Classification Product Code: KOE
Date Received: 07/03/1996
Decision Date: 10/21/1996
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: BARD EAGLE INFLATION DEVICE
Manufacturer: RYDER INTL. CORP.
Device Classification Name: dilator, urethral
Regulation Number: 876.5520
Classification Product Code: KOE
Date Received: 07/03/1996
Decision Date: 10/21/1996
Regulation Medical Specialty: Gastroenterology/Urology
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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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