KIO
1989-04-04
Slide Stainer, Immersion Type
FDA product code KIO · 1 cleared devices
Class 1
Pathology
- Regulation
- 21 CFR 864.3800
- Review panel
- PA
- Implant
- No
- Life sustaining
- No
- Third party review
- No
- GMP exempt
- No
- Clearance span
- 1989-04-04 – 1989-04-04
No matching devices.
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