Medical Device Manufacturer · US , Longmont , CO

Staodyne, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1992

Total

Cleared

Denied

Staodyne, Inc. has 9 FDA 510(k) cleared medical devices. Based in Longmont, US.

Historical record: 9 cleared submissions from 1992 to 1995. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Staodyne, Inc. Filter by specialty or product code using the sidebar.

Staodyne, 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 - Staodyne, Inc.

9 devices

1-9 of 9

Cleared Dec 04, 1995

VARAPULSE-2

K952680 · IPF

Physical Medicine · 175d

Cleared Jun 02, 1995

STERILE TREATMENT ELECTRODE

K941923 · GZJ

Neurology · 408d

Cleared Aug 16, 1993

TPK CUTANEOUS ELECTRODE

Physical Medicine · 224d

MODEL 19 STIMULATOR, NERVE, TRANSCUTANEOUS

Physical Medicine · 117d

Staodyne, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Staodyne, Inc.

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