Product Code: PXG FDA class 1 21 CFR 880.6890

Spill Kit

General Hospital

The Spill Kit is a general hospital convenience kit containing absorbents, personal protective equipment, and disposal containers used for the safe containment and cleanup of medical or biological fluid spills in a healthcare setting, reducing risk of contamination and exposure. Product code PXG is established as a convenience kit under FDA's 1997 Convenience Kits Interim Regulatory Guidance and is under enforcement discretion, not requiring a 510(k) if all guidance criteria are met. It is classified as FDA Class I under regulation 21 CFR 880.6890, subject only to general controls. It falls under the General Hospital medical specialty and is not flagged as an implant or life-sustaining device.

510(k)s
0
FEI Numbers
15
Registration Numbers
15
Unique Applicants
0
Years Active

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Basic Information

Product Code
PXG
Device Class
FDA class 1
Regulation Number
880.6890
Medical Specialty
General Hospital
Review Panel
HO
Submission Type
7

Device Characteristics

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

Definition

This product code has been established in accordance with the May 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080217.pdf. This type of convenience kit, as listed in the guidance above, is under enforcement discretion, and does not require a premarket notification (510(k)) to market if it meets all criteria in the guidance.

FEI Numbers

This FDA classification entry is associated with 15 FEI numbers. Click on an entry to view related FDA registrations.

Registration Numbers

This FDA classification entry is associated with 15 registration numbers. Click on an entry to view related FDA registrations.