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

Table, Obstetric (And Accessories)

21 CFR 884.4900 / Obstetrics/Gynecology
FDA source (opens on fda.gov)

KNC is the FDA product code for Table, Obstetric (And Accessories), a class II device type, regulated under 21 CFR 884.4900. As of , FDA records hold 26 510(k) clearances under this code, the most recent dated , and 12 recalls.

Classification record

Product code
KNC
Device name
Table, Obstetric (And Accessories)
Regulation
21 CFR 884.4900
Device class
Class II
Review panel
Obstetrics/Gynecology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
26
Ingested recalls
12

Clearances, product code KNC

By decision year
26 clearances under product code KNC with a decision year between 1977 and 2000, 1983 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code KNC by decision year
YearClearances
19771
19791
19802
19812
19821
19834
19841
19853
19862
19872
19891
19901
19933
19941
20001

Applicants with the most clearances

Product code KNC
Applicants holding the most 510(k) clearances under product code KNC
ApplicantClearances
Adel Medical, Ltd.3
Hill-Rom Inc.2
AD-Tech Medical Instrument Corp.1
Amsco Co.1
Amsco Sterile Recoveries, Inc.1
Buckman Co., Inc.1
Century Manufacturing Co.1
Daun International, Inc.1
Ets Rene Marzet1
Global Medical Prods, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code