FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
L12 LED Light Source with AIM
K Number: K260108
·
Decision Feb 12, 2026
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
60
Applicant Total
101
Review Days
29
Basic Information
- Device Name
- L12 LED Light Source with AIM
- K Number
- K260108
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 876.1500
- Medical Specialty
- Gastroenterology, Urology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Stryker Endoscopy
- Date Received
- January 14, 2026
- Decision Date
- February 12, 2026
- Product Code
- OWN
- Advisory Committee
- Gastroenterology, Urology
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OWN | Confocal Optical Imaging | FDA class 2 | Gastroenterology, Urology |
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