Processor, Tissue, Automated
FDA product code IEO · 12 cleared devices
Class 1
Pathology
- Regulation
- 21 CFR 864.3875
- Review panel
- PA
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1977-03-07 – 1992-12-29
IEO
1992-12-29
IEO
1988-09-02
LX-80 AUTOMATED TISSUE PROCESSOR (PLASTIC)
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IEO
1988-07-01
SAKURA HEM-480 ELECTRON MICROSCOPY PROCESSOR
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IEO
1985-10-10
LX 300 TISSUE PROCESSOR
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IEO
1985-05-15
LX120 TISSUE PROCESSOR
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IEO
1984-11-30
LKB 2189 ULTROPROCESSOR
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IEO
1984-02-04
AUTOTECHNICON V TISSUE PROCESS SYS
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IEO
1983-07-28
TISSUE-TEK V.I.P. 100/200
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IEO
1980-07-28
TISSUE PROCESSING SYSTEM
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IEO
1980-07-28
TISSUE-TEK III MINI-RAPID PROCESSOR
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IEO
1977-08-22
TISSUE-TEK III V.I.P.
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IEO
1977-03-07
HISTO-TEK W/ AUTOMATIC COVERSLIPPER
View details →No matching devices.
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