ClearanceBrief
Company ยท US

Machida America, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1988. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EQNLaryngoscope, Nasopharyngoscope4
EOQBronchoscope (Flexible Or Rigid)2
HRXArthroscope1
NVEWasher, Cleaner, Automated, Endoscope1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jan 14, 1988K871712MACHIDA AMERICA MODEL AC-5000 AUTOMATIC DISINFECT.
Machida America, Inc.
NVE
Feb 28, 1986K854581MACHIDA SEMI-RIGID BRONCHOSCOPE FBS-6R-50
Machida America, Inc.
EOQ
Jun 11, 1985K844834MACHIDA FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE FNS-1
Machida America, Inc.
EOQ
May 16, 1984K841087FLEXIBLE ORTHOPEDIC ENDOSCOPE ICA-1000
Machida America, Inc.
HRX
May 13, 1982K821182MODEL ENT-4L-FLEXIBLE NASOPHARYNGO-
Machida America, Inc.
EQN
May 13, 1982K821181FLEXIBLE NASOPHARYNGO-LARYNGOSCOPE #
Machida America, Inc.
EQN
Oct 19, 1981K812734MACHIDA FLEXIBLE INTUBATION SCOPE FLS-P
Machida America, Inc.
EQN
Jul 28, 1981K811943MACHIDA NASOPHARYNGO-LARYNGOSCOPE
Machida America, Inc.
EQN

Latest recalls

DateFirm and productCodeLinked 510(k)
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