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

Table, Mechanical

21 CFR 890.3750 / Physical Medicine
FDA source (opens on fda.gov)

INW is the FDA product code for Table, Mechanical, a class I device type, regulated under 21 CFR 890.3750. As of , FDA records hold 35 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
INW
Device name
Table, Mechanical
Regulation
21 CFR 890.3750
Device class
Class I
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
35
Ingested recalls
1

Clearances, product code INW

By decision year
35 clearances under product code INW with a decision year between 1978 and 1994, 1989 the highest year at 8.
Show the numbers
510(k) clearances under FDA product code INW by decision year
YearClearances
19781
19801
19812
19821
19863
19882
19898
19903
19922
19937
19945

Applicants with the most clearances

Product code INW
Applicants holding the most 510(k) clearances under product code INW
ApplicantClearances
Bailey Mfg. Co.4
Rifton Equipment for the Handicapped4
James Leckey Design Ltd2
Progressive Electrical Therapeutics2
Titan Tables2
Avratronics Corp.1
Camp Intl., Inc.1
Chattanooga Group, Inc.1
Cozcon, Inc.1
Fred Sammons, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 101 companies shown, in name order