FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
TECHNA VISION, INC.ELECTRIC TABLE
K Number: K853744
·
Decision Oct 17, 1985
Classifications
1
FEI Numbers
54
Registration Numbers
55
Same Product Code
6
Applicant Total
4
Review Days
41
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
- TECHNA VISION, INC.ELECTRIC TABLE
- K Number
- K853744
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 886.4855
- Medical Specialty
- Ophthalmic
- Decision
- Substantially Equivalent
- Applicant
- Techna Vision
- Date Received
- September 6, 1985
- Decision Date
- October 17, 1985
- Product Code
- HRJ
- 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 |
|---|---|---|---|
| HRJ | Table, Instrument, Powered, Ophthalmic | FDA class 1 | Ophthalmic |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (HRJ), ordered by most recent decision date.
MARCO H AND TS-1 INSTRUMENT TABLES
FDA 510(k)
FDA Class 1
·Ophthalmic
910T MONTORIZED INSTRUMENT TABLE
FDA 510(k)
FDA Class 1
·Ophthalmic
TBD, LENS MEASURING DEVICE
FDA 510(k)
FDA Class 1
·Ophthalmic
RELIANCE 1379
FDA 510(k)
FDA Class 1
·Ophthalmic
WOODLYN CLASSIC INSTRUMENT STAND
FDA 510(k)
FDA Class 1
·Ophthalmic
MACHEMER/TANO ROTATING
FDA 510(k)
FDA Class 1
·Ophthalmic