IDO
1987-01-05
Microtome, Rotary
FDA product code IDO · 5 cleared devices
Class 1
Pathology
- Regulation
- 21 CFR 864.3010
- Review panel
- PA
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- Yes
- Clearance span
- 1981-08-18 – 1987-01-05
IDO
1986-09-19
ROTARY MICROTOME
View details →
IDO
1984-11-30
LKB 2230 ROTARY ONE
View details →
IDO
1981-09-29
TISSUE-TEK III ACCU-CUT ROTARY MICROTOME
View details →
IDO
1981-08-18
LKB-BROMMA 2218 HISTORANGE MICROTOME
View details →No matching devices.
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