# K960700: Logiq  A200 Diagnostic Ultrasound System

- Pathway: 510(k) (Traditional)
- Applicant: GE Medical Systems
- Decided: Aug 28, 1996 after 190 days
- Product code: IYO (System, Imaging, Pulsed Echo, Ultrasonic)
- Device class: 2
- Regulation: 21 CFR 892.1560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K863700 (1987). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K863700: RT2800(115V)/H4008C and RT2800(220/240V)/H4008CE, General Electric Co. (1987). Our OCR of the scanned summary read K873700, FDA’s number for Institutional Bili Light (Ibl) (Physician Engineered Products, Inc.). Corrected to the number one digit away whose FDA name carries the summary’s words for the device, “GE Medical Systems RT2800 diagnostic ultrasound system”.

## Most influential descendants
- K992208: GE Logiq 200 MD Diagnostic Ultrasound System (1999), 0 descendants of its own

## Indications for use
The LOGIQ «200 diagnostic ultrasound system is intended for use in diagnostic ultrasound imaging using B, M, and B/M combination modes in the following areas: Fetal Abdominal Intraoperative Pediatric Small organs including breast, neck, chest, male and female reproductive organs, limbs, and extremities Adult Cephalic Neonatal cephalic Adult cardiac Pediatric cardiac Trans-vaginal Trans-rectal

Source page: https://510kreport.com/device/K960700
Methodology: https://510kreport.com/methodology