Medical Device Manufacturer · US , San Jose , CA

Helio Medical Supplies, Inc. - FDA 510(k) Cleared Devices

12 submissions · 12 cleared · Since 1996

Total

Cleared

Denied

Helio Medical Supplies, Inc. has 12 FDA 510(k) cleared general hospital devices. Based in San Jose, US.

Historical record: 12 cleared submissions from 1996 to 2008.

Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.

Helio Medical Supplies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Helio Medical Supplies, Inc.

12 devices

1-12 of 12

BRIO ACUPUNCTURE NEEDLES

K072778 · MQX

General Hospital · 52d

Cleared Sep 20, 2006

LYRA ACUPUNCTURE NEEDLES

K062448 · MQX

General Hospital · 29d

Cleared Jan 13, 2006

SEVEN STAR NEEDLE

K052723 · MQX

General Hospital · 106d

Cleared Mar 25, 2005

PRESS TACK/INTRADERMAL ACUPUNCTURE NEEDLES

K050295 · MQX

General Hospital · 46d

Cleared Feb 08, 2005

C&G ACUPUNCTURE NEEDLE

K043277 · MQX

General Hospital · 74d

Cleared Apr 14, 2003

VINCO BRAND ACUPUNCTURE NEEDLE

K024207 · MQX

General Hospital · 115d

Cleared Dec 11, 2001

ACUGLIDE BRAND ACUPUNCTURE NEEDLES

K012583 · MQX

General Hospital · 123d

Cleared Aug 27, 1999

KANGNIAN BRAND ACUPUNCTURE NEEDLE

K991507 · MQX

General Hospital · 120d

Cleared Aug 27, 1999

ACUMASTER BRAND ACUPUNCTURE NEEDLE

K991508 · MQX

General Hospital · 120d

Cleared Jul 03, 1996

CARBO BRAND/VIVA BRAND ACUPUNCTURE NEEDLES

K961339 · MQX

General Hospital · 86d

Cleared Jun 06, 1996

FIRARD II/ TDP LAMP

K960036 · ILY

Physical Medicine · 156d

Helio Medical Supplies, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Helio Medical Supplies, Inc.

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