Product code KEW— Pathology
ABCO ULTRA SLIDE MICROSCOPE SLIDE
- Classification name
- Slides, Microscope
- Device class
- Class 1
- Regulation
- 21 CFR 864.3010
- Advisory panel
- Pathology
- Total cleared
- 8
- First cleared
- Most recent
Market context for product code KEW
FDA has cleared devices under product code KEW between 1976 and 1989, filed by 7 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
- 1988
- 1983
- 1982
- 1981
- 1980
- 1976
Top applicants under product code KEW
Recent clearances under product code KEW
- K891604 — THE CEN-SLIDE(TM) CENTRIFUGE TUBE
- K890042 — MICROSCOPE SLIDES PRECOATED
- K882357 — MICROSCOPE SLIDES PRECOATED W/HISTOGRIP & POLY-LY
- K831065 — SECTIONING AID KIT
- K820100 — FROSTED GLASS SLIDES
- K813242 — QUANTIMETRIC 2 TEST KIT
- K800232 — ABCO ULTRA SLIDE MICROSCOPE SLIDE
- K760278 — SLIDE, LAB-TEK COVERED MICRO
Data sourced from openFDA. This site is unofficial and independent of the FDA.