Helio Medical Supplies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K080221 | EA STIMULATOR | September 9, 2008 |
| K072778 | BRIO ACUPUNCTURE NEEDLES | November 19, 2007 |
| K062448 | LYRA ACUPUNCTURE NEEDLES | September 20, 2006 |
| K052723 | SEVEN STAR NEEDLE | January 13, 2006 |
| K050295 | PRESS TACK/INTRADERMAL ACUPUNCTURE NEEDLES | March 25, 2005 |
| K043277 | C&G ACUPUNCTURE NEEDLE | February 8, 2005 |
| K024207 | VINCO BRAND ACUPUNCTURE NEEDLE | April 14, 2003 |
| K012583 | ACUGLIDE BRAND ACUPUNCTURE NEEDLES | December 11, 2001 |
| K991508 | ACUMASTER BRAND ACUPUNCTURE NEEDLE | August 27, 1999 |
| K991507 | KANGNIAN BRAND ACUPUNCTURE NEEDLE | August 27, 1999 |
| K961339 | CARBO BRAND/VIVA BRAND ACUPUNCTURE NEEDLES | July 3, 1996 |
| K960036 | FIRARD II/ TDP LAMP | June 6, 1996 |