FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
MILLER/NADLER GLARE TESTER
K Number: K812706
·
Decision Nov 16, 1981
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
8
Applicant Total
1
Review Days
53
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- MILLER/NADLER GLARE TESTER
- K Number
- K812706
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.1680
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Mosebach Electric & Supply
- Date Received
- September 24, 1981
- Decision Date
- November 16, 1981
- Product Code
- HOS
- 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 |
|---|---|---|---|
| HOS | Projector, Ophthalmic | FDA class 1 | Ophthalmic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HOS), ordered by most recent decision date.
WIRELESS CHART PROJECTOR,HCP-W 721
FDA 510(k)
FDA Class 1
·Ophthalmic
MARCO CP-600 AUTO CHART PROJECTOR/CP-1 CHART PROJE
FDA 510(k)
FDA Class 1
·Ophthalmic
BURTON PROJECTOR HEAD - MODEL 6000-H
FDA 510(k)
FDA Class 1
·Ophthalmic
OPHTHALMIC PROJECTOR
FDA 510(k)
FDA Class 1
·Ophthalmic
WOODLYN OPHTHALMIC PROJECTOR
FDA 510(k)
FDA Class 1
·Ophthalmic
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR
FDA 510(k)
FDA Class 1
·Ophthalmic