Fonar Corp.
Fonar Corp. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2006.
Top product codes for Fonar Corp.
Recent clearances by Fonar Corp.
- K061930 — INDOMITABLE MAGNETIC RESONANCE IMAGING SCANNER ACCESSORY
- K011485 — PINNACLE MAGNETIC RESONANCE IMAGING SCANNER
- K003453 — SYMPULSE COMPUTER SYSTEM FOR FONAR MRI SCANNERS
- K002490 — INDOMITABLE MAGNETIC RESONANCE IMAGING SCANNER
- K994287 — FONAR 360 DEGREE MAGNETIC RESONANCE IMAGING SCANNER
- K951681 — QUAD 1200 MAGNETIC RESONANCE IMAGING SCANNER
- K940772 — ECHO(TM) (QUAD(TM) 7000 MAGNETIC RESONANCE IMAGING SCANNER)
- K920789 — B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER
- K915567 — MAGNETIC RESONANCE DIAGNOSTIC DEVICE(ACCESORY)
- K910839 — ULTIMATE 3000
- K883699 — B3000/B3000M MAGNETIC RESONANCE IMAGING SCANNER
- K883648 — BETA 3000M MOBILE NMR IMAGING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.