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FDA 510(k), K812558, TISSUE-TEK III ACCU-CUT ROTARY MICROTOME
FDA 510(k), K812558, TISSUE-TEK III ACCU-CUT ROTARY MICROTOME
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510(K) Number: K812558
Device Name: TISSUE-TEK III ACCU-CUT ROTARY MICROTOME
Manufacturer: MILES LABORATORIES, INC.
Device Classification Name: Microtome, Rotary
Regulation Number: 864.3010
Classification Product Code: IDO
Date Received: 09/08/1981
Decision Date: 09/29/1981
Regulation Medical Specialty: Pathology
Device Name: TISSUE-TEK III ACCU-CUT ROTARY MICROTOME
Manufacturer: MILES LABORATORIES, INC.
Device Classification Name: Microtome, Rotary
Regulation Number: 864.3010
Classification Product Code: IDO
Date Received: 09/08/1981
Decision Date: 09/29/1981
Regulation Medical Specialty: Pathology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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