Medical Device Manufacturer · US , Mchenry , IL

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

49 submissions · 47 cleared · Since 1977

Total

Cleared

Denied

Medical Devices, Inc. has 47 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 47 cleared submissions from 1977 to 2001. Primary specialty: Neurology.

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

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

49 devices

1-12 of 49

Cleared Feb 05, 2001

PAD PRO PEDIATRIC ELECTRODE, MODEL PAD PRO 2602

K002280 · MKJ

Cardiovascular · 194d

HOME MICROCURRENT HMC

XENON ENDOSCOPIC ILLUMINATOR, MODEL XEI-300

K924897 · GCT

Gastroenterology & Urology · 280d

Cleared May 17, 1993

VIDEO CAMERA W/ ELECTRONIC SHUTTER MODEL VCE-10

K930053 · FWF

General & Plastic Surgery · 131d

Cleared Nov 06, 1992

IF-II (TM), MODEL 7200

K923914 · IPF

Physical Medicine · 98d

Cleared Jul 21, 1992

MEDITRON AUTOMATIC ELECTRONIC INSUFF. MODEL AEI-15

K920071 · GEI

General & Plastic Surgery · 196d

Cleared Jun 18, 1992

MEDITRON ELECTRONIC LAPAROSCOPIC INSUFFLATOR

K915694 · HIF

Obstetrics & Gynecology · 178d

Cleared Mar 11, 1992

BIPOLAR ENDOSTASIS PROBE, BEST (TM)

K915408 · KNS

Gastroenterology & Urology · 100d

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

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