Minivisor Terminal
by Organon Teknika Corp. 510(k)
Active
510(k) K802263
Overview
The Minivisor Terminal is a System, Imaging, Pulsed Echo, Ultrasonic device classified under product code IYO. It is a Class II ultrasound system.
It was cleared by the FDA via the 510(k) pathway under K802263 on October 31, 1980, following a traditional review. The device is used in radiology and was submitted by Organon Teknika Corp. from McHenry, Illinois.
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK802263 | Date31 Oct 1980 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — FDA 510(k) Active
Recalls
No FDA recalls on record, checked 22 Oct 2026.
Specification
- 510(k) Number
- FDA Product Code
- IYO
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.1560
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Other devices from Organon Teknika Corp.
Questions
What is the Minivisor Terminal used for?
The Minivisor Terminal is a pulsed echo ultrasonic imaging system intended for use in radiology, as indicated by its product code IYO and classification under advisory committee RA (Radiology).
How was the Minivisor Terminal cleared for market?
The Minivisor Terminal received FDA clearance through the traditional 510(k) pathway under submission K802263, with a decision date of October 31, 1980, based on a finding of substantial equivalence (SESE).
Who manufactures the Minivisor Terminal and where are they located?
The Minivisor Terminal is manufactured by Organon Teknika Corp., located at 803 N. Front St. Suite 3, McHenry, Illinois, 60050, United States.