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FDA 510(k), K040390, STRYKER UROLOGY AND GYNECOLOGY HARDWARE SYSTEM
FDA 510(k), K040390, STRYKER UROLOGY AND GYNECOLOGY HARDWARE SYSTEM
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510(K) Number: K040390
Device Name: STRYKER UROLOGY AND GYNECOLOGY HARDWARE SYSTEM
Manufacturer: Stryker Endoscopy
Device Classification Name: hysteroscope (and accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 02/17/2004
Decision Date: 05/17/2004
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: STRYKER UROLOGY AND GYNECOLOGY HARDWARE SYSTEM
Manufacturer: Stryker Endoscopy
Device Classification Name: hysteroscope (and accessories)
Regulation Number: 884.1690
Classification Product Code: HIH
Date Received: 02/17/2004
Decision Date: 05/17/2004
Regulation Medical Specialty: Obstetrics/Gynecology
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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