Product code KEO— Pathology
BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
- Classification name
- Formulations, Paraffin, All
- Device class
- Class 1
- Regulation
- 21 CFR 864.4010
- Advisory panel
- Pathology
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code KEO
FDA has cleared devices under product code KEO between 1976 and 1989, filed by 9 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1989
- 1986
- 1984
- 1983
- 1981
- 1976
Top applicants under product code KEO
Recent clearances under product code KEO
- K893772 — TISSUE EMBEDDING MEDIUM
- K862223 — MICRO THIN* PARAFFIN
- K862141 — HISTOLOGY PARAFFIN
- K861270 — BLUE RIBBON PARAFFIN INFILTRATION/EMBEDDING MED.
- K842053 — PARAPLAST EXTRA TISSUE EMBEDDING MED.
- K833071 — TECHNICON PARACUT
- K831580 — PARAFFIN INFILTRATION MEDIUM
- K812191 — VASPAR SEALENT
- K810568 — PARAFFIN EMBEDDING MEDIUM
- K803241 — HISTOLOGICAL EMBEDDING MEDIA
- K760602 — SORVALL EMBEDDING MEDIUM
Data sourced from openFDA. This site is unofficial and independent of the FDA.