Medical Device Manufacturer · US , Mchenry , IL

Kelleher Corp. - FDA 510(k) Cleared Devices

94 submissions · 94 cleared · Since 1982

Total

Cleared

Denied

Kelleher Corp. has 94 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 94 cleared submissions from 1982 to 1983. Primary specialty: Ear, Nose, Throat.

Browse the FDA 510(k) cleared devices submitted by Kelleher Corp. Filter by specialty or product code using the sidebar.

Kelleher Corp. 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 - Kelleher Corp.

94 devices

1-12 of 94

Cleared Jan 28, 1983

NAGASHIMA NS-III ELECTRONYSTAGMOGRAPH

K822268 · GWN

Neurology · 183d

Cleared Jan 28, 1983

EMERGENCY TRACHEOSTOMY INSTRUMENT SET

K822618 · LJW

Ear, Nose, Throat · 148d

Cleared Dec 07, 1982

ELECTROSURGICAL UNIT

K823083 · GEI

General & Plastic Surgery · 49d

Cleared Nov 22, 1982

ENT TREATMENT UNITS

K822252 · ETF

Ear, Nose, Throat · 116d

HEAD MIRRORS W/HEAD LAMPS & HEAD BANDS

K822272 · HPQ

Ophthalmic · 104d

Cleared Oct 27, 1982

TYMPANOSTOMY TUBES & VARIOUS TYPES

K822017 · ETD

Ear, Nose, Throat · 111d

Cleared Oct 26, 1982

VARIOUS TYPES OF LIGHT SOURCE HANDLES

K822257 · EOQ

Ear, Nose, Throat · 89d

Cleared Oct 22, 1982

LARYNGEAL SPATULAS

K822259 · EQH

Ear, Nose, Throat · 85d

Cleared Oct 20, 1982

FACE SHIELDS

K822004 · KNT

Gastroenterology & Urology · 104d

Cleared Oct 18, 1982

LARYNGEAL SYRINGE

K822185 · FMF

General Hospital · 87d

Cleared Oct 13, 1982

NAGASHIMA SN OPERATOR'S CHAIR

K822264 · GBB

General & Plastic Surgery · 76d

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Kelleher Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kelleher Corp.

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