510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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INOClass II

Chair, Positioning, Electric

21 CFR 890.3110 / Physical Medicine
FDA source (opens on fda.gov)

INO is the FDA product code for Chair, Positioning, Electric, a class II device type, regulated under 21 CFR 890.3110. As of , FDA records hold 53 510(k) clearances under this code, the most recent dated , and 5 recalls.

Classification record

Product code
INO
Device name
Chair, Positioning, Electric
Regulation
21 CFR 890.3110
Device class
Class II
Review panel
Physical Medicine
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
53
Ingested recalls
5

Clearances, product code INO

By decision year
53 clearances under product code INO with a decision year between 1978 and 2014, 1988 the highest year at 6.
Show the numbers
510(k) clearances under FDA product code INO by decision year
YearClearances
19781
19801
19821
19831
19855
19864
19886
19903
19911
19934
19941
19952
19961
19981
19991
20003
20022
20031
20062
20072
20082
20094
20101
20111
20131
20141

Applicants with the most clearances

Product code INO
Applicants holding the most 510(k) clearances under product code INO
ApplicantClearances
Invacare GmbH4
Altimate Medical, Inc.2
Craftmatic/Contour Organization, Inc.2
Fresenius Medical Care South Asia Pacific Pty, Ltd.2
Penox Technologies, Inc.2
Pride Health Care Equipment2
Pride Health Care, Inc.2
Pride Mobility Products Corp2
Action Engineering, Inc.1
Alc, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 50 companies shown, in name order