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FDA 510(k), K971849, CYTOLOGY BRUSH
FDA 510(k), K971849, CYTOLOGY BRUSH
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510(K) Number: K971849
Device Name: CYTOLOGY BRUSH
Manufacturer: TEAM TECHNOLOGIES, INC.
Device Classification Name: spatula, cervical, cytological
Regulation Number: 884.4530
Classification Product Code: HHT
Date Received: 05/19/1997
Decision Date: 07/24/1997
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: CYTOLOGY BRUSH
Manufacturer: TEAM TECHNOLOGIES, INC.
Device Classification Name: spatula, cervical, cytological
Regulation Number: 884.4530
Classification Product Code: HHT
Date Received: 05/19/1997
Decision Date: 07/24/1997
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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