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FDA 510(k), K972074, SUCTION INSTRUMENTATION
FDA 510(k), K972074, SUCTION INSTRUMENTATION
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510(K) Number: K972074
Device Name: SUCTION INSTRUMENTATION
Manufacturer: WALTER LORENZ SURGICAL, INC.
Device Classification Name: apparatus, suction, operating-room, wall vacuum powered
Regulation Number: 880.6740
Classification Product Code: GCX
Date Received: 06/03/1997
Decision Date: 07/25/1997
Regulation Medical Specialty: General Hospital
Device Name: SUCTION INSTRUMENTATION
Manufacturer: WALTER LORENZ SURGICAL, INC.
Device Classification Name: apparatus, suction, operating-room, wall vacuum powered
Regulation Number: 880.6740
Classification Product Code: GCX
Date Received: 06/03/1997
Decision Date: 07/25/1997
Regulation Medical Specialty: General Hospital
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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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