FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CONFOSCAN
K Number: K971953
·
Decision Aug 14, 1997
Classifications
1
FEI Numbers
54
Registration Numbers
55
Same Product Code
107
Applicant Total
9
Review Days
78
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Basic Information
- Device Name
- CONFOSCAN
- K Number
- K971953
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 886.1850
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Tomey Corporation USA
- Date Received
- May 28, 1997
- Decision Date
- August 14, 1997
- Product Code
- HJO
- Advisory Committee
- Ophthalmic
- Review Advisory Committee
- OP
- 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 |
|---|---|---|---|
| HJO | Biomicroscope, Slit-Lamp, Ac-Powered | FDA class 2 | Ophthalmic |
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Other Clearances by Tomey Corporation USA
| K Number | Device Name | ||
|---|---|---|---|
| K971685 | IMAGESCAPE DIGITAL RETINAL IMAGE SYSTEM | Jun 24, 1997 | Substantially Equivalent |
| K961805 | TOMEY DTL ELECTRODE | May 9, 1997 | Substantially Equivalent |
| K932571 | TOMEY PE-400 PORTABLE ERG & VEP WITH OPTIONAL PS-4 | Aug 31, 1995 | Substantially Equivalent |
| K945959 | VIDEO VISION ANALYZER (VIVA), VRB 100 | Mar 1, 1995 | Substantially Equivalent |
| K944910 | TOMEY EM-1000 SPECULAR MICROSCOPE | Nov 22, 1994 | Substantially Equivalent |
| K924760 | TOMEY PROTON TONOMETER | Apr 5, 1993 | Substantially Equivalent |
| K921815 | TOMEY PE-300 PORTABLE ERG | Jul 15, 1992 | Substantially Equivalent |
| K912112 | PF-400,GF-300,IF-200,PG400,PG400C,AND ED-480 | Jun 17, 1991 | Substantially Equivalent |