Multigon Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K052067 | DOPPLER GUIDED PROCTOSCOPE, MODEL 500H | August 29, 2005 |
| K051739 | POCKET TRANSCRANIAL AND VASCULAR DOPPLER SPECTRUM ANALYZER, MODEL 500P; PW DOPPLER ULTRAOUND PROBE, | July 28, 2005 |
| K912044 | MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATOR | June 24, 1991 |
| K881263 | MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLER | January 5, 1990 |
| K882755 | MODEL 500V VASCULAR SPECTRUM ANALYZER | November 29, 1988 |
| K863589 | MODEL 600 VASCULAR DUPLEX IMAGER | June 24, 1987 |
| K860435 | MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER | May 5, 1986 |
| K852680 | TRITON LAPAROSCOPIC COAGULATOR INSUFFLATOR & LAVAG | December 23, 1985 |