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

Container, Liquid Medication, Graduated

21 CFR 880.6430 / General Hospital
FDA source (opens on fda.gov)

KYW is the FDA product code for Container, Liquid Medication, Graduated, a class I device type, regulated under 21 CFR 880.6430. As of , FDA records hold 2 510(k) clearances under this code, the most recent dated , and 13 recalls.

Classification record

Product code
KYW
Device name
Container, Liquid Medication, Graduated
Regulation
21 CFR 880.6430
Device class
Class I
Review panel
General Hospital
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
2
Ingested recalls
13

Clearances, product code KYW

By decision year
2 clearances under product code KYW with a decision year between 1979 and 1980, 1979 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code KYW by decision year
YearClearances
19791
19801

Applicants with the most clearances

Product code KYW
Applicants holding the most 510(k) clearances under product code KYW
ApplicantClearances
Cutter Laboratories, Inc.1
General Clinical Plastics Corp.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 194 companies shown, in name order