Medical Device Manufacturer · US , Walker , MI

Eder Instrument Co, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 1979

Total

Cleared

Denied

Eder Instrument Co, Inc. has 10 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 10 cleared submissions from 1979 to 1984. Primary specialty: General & Plastic Surgery.

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

Eder Instrument Co, 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 - Eder Instrument Co, Inc.

10 devices

1-10 of 10

Cleared Dec 14, 1984

BIPOLAR SUCTION ELECTRODE

K843498 · GET

General & Plastic Surgery · 99d

Cleared Oct 31, 1984

SURGICAL KNIVES & PROBES

K843497 · EMF

General & Plastic Surgery · 55d

Cleared Oct 31, 1984

ARTHROSCOPY LEG HOLDER

K843499

General & Plastic Surgery · 55d

Cleared Sep 12, 1983

LARYNGOSCOPE ATTACHMENT PH2000

K831255 · EQN

Ear, Nose, Throat · 147d

Cleared Jul 26, 1983

LASER BRONCHOSCOPE

K831240 · EOQ

Ear, Nose, Throat · 102d

Cleared Jun 10, 1983

LASER LAPARAXOPE

K831241 · HET

Obstetrics & Gynecology · 56d

Cleared Oct 22, 1982

ENDOSCOPIC VIDEOSYSTEM

K822959 · FET

Gastroenterology & Urology · 17d

Cleared Oct 31, 1980

SURGICAL KNIVES & PROBES

K802479 · HXB

Orthopedic · 24d

Cleared Nov 13, 1979

GRASPING FORCEP (W/FOUR PRONGS)

K792100 · GEN

General & Plastic Surgery · 25d

Cleared Aug 03, 1979

ENDOSCOPIC INSTRUMENT

K791052 · HET

Obstetrics & Gynecology · 58d

Eder Instrument Co, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Eder Instrument Co, Inc.

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