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

Table, Cystometric, Non-Electric And Accessories

21 CFR 876.4890 / Gastroenterology, Urology
FDA source (opens on fda.gov)

KQS is the FDA product code for Table, Cystometric, Non-Electric And Accessories, a class I device type, regulated under 21 CFR 876.4890. As of , FDA records hold 8 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
KQS
Device name
Table, Cystometric, Non-Electric And Accessories
Regulation
21 CFR 876.4890
Device class
Class I
Review panel
Gastroenterology, Urology
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
8
Ingested recalls
0

Clearances, product code KQS

By decision year
8 clearances under product code KQS with a decision year between 1976 and 1995, 1986 the highest year at 2.
Show the numbers
510(k) clearances under FDA product code KQS by decision year
YearClearances
19761
19791
19801
19851
19862
19871
19951

Applicants with the most clearances

Product code KQS
Applicants holding the most 510(k) clearances under product code KQS
ApplicantClearances
American Sterilizer Co.2
Mallinckrodt Group, Inc.2
Dornier Medtech America, Inc.1
Oec-Diasonics, Inc.1
Siemens Corp.1
Sybron Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code