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FDA 510(k), K060233, TROKAMED GMBH ENDOSCOPES AND ACCESSORIES
FDA 510(k), K060233, TROKAMED GMBH ENDOSCOPES AND ACCESSORIES
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510(K) Number: K060233
Device Name: TROKAMED GMBH ENDOSCOPES AND ACCESSORIES
Manufacturer: TROKAMED GMBH
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/30/2006
Decision Date: 07/19/2006
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: TROKAMED GMBH ENDOSCOPES AND ACCESSORIES
Manufacturer: TROKAMED GMBH
Device Classification Name: laparoscope, general & plastic surgery
Regulation Number: 876.1500
Classification Product Code: GCJ
Date Received: 01/30/2006
Decision Date: 07/19/2006
Regulation Medical Specialty: Gastroenterology/Urology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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