Medical Device Manufacturer · US , Mchenry , IL

Machida America, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1981

8

Total

8

Cleared

0

Denied

Machida America, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1981 to 1988. Primary specialty: Ear, Nose, Throat.

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

FDA 510(k) Regulatory Record - Machida America, Inc.

8 devices

1-8 of 8

Cleared Jan 14, 1988

MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.

General Hospital · 255d

Cleared Feb 28, 1986

MACHIDA SEMI-RIGID BRONCHOSCOPE FBS-6R-50

Ear, Nose, Throat · 105d

Cleared Jun 11, 1985

MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1

Ear, Nose, Throat · 181d

Cleared May 16, 1984

FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000

Orthopedic · 64d

Cleared May 13, 1982

FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #

Ear, Nose, Throat · 16d

Cleared May 13, 1982

MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-

Ear, Nose, Throat · 16d

Cleared Oct 19, 1981

MACHIDA FLEXIBLE INTUBATION SCOPE FLS-P

Ear, Nose, Throat · 20d

Cleared Jul 28, 1981

MACHIDA NASOPHARYNGO-LARYNGOSCOPE

Ear, Nose, Throat · 21d