Product Code: KYW FDA class 1 21 CFR 880.6430

Container, Liquid Medication, Graduated

General Hospital

The Graduated Liquid Medication Container is a general-purpose vessel marked with volume graduations used to measure and store liquid medications for administration to patients in clinical or home settings. It is classified as FDA Class 1, the lowest risk category, subject to general controls only, and is exempt from Good Manufacturing Practice (GMP) requirements. The product code is KYW, regulated under 21 CFR 880.6430, in the General Hospital medical specialty. This device is GMP exempt.

510(k)s
2
FEI Numbers
208
Registration Numbers
208
Unique Applicants
2
Years Active
1

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Basic Information

Product Code
KYW
Device Class
FDA class 1
Regulation Number
880.6430
Medical Specialty
General Hospital
Review Panel
HO
Submission Type
4

Device Characteristics

GMP Exempt
Implant
Life Sustain/Support
Third Party
Summary Malfunction Reporting

510(k) Clearance History

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Related 510(k) Clearances

This FDA classification is associated with 2 510(k) clearances via K numbers.

K Number Device Name
K800213 PHARMACY ADDITIVE SYRINGE SET
K791345 MEDICINE CUP

FEI Numbers

This FDA classification entry is associated with 208 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 208 registration numbers. Click on an entry to view related FDA registrations.