510(k) K901179

ENEMA BUCKET SET by Orion Life Systems, Inc. — Product Code FCE

K901179 is an FDA 510(k) premarket notification submitted by Orion Life Systems, Inc. for the device "ENEMA BUCKET SET". The FDA issued a decision of Substantially Equivalent (kit) on June 28, 1990. The device falls under product code FCE (Enema Kit), a Class I device regulated under 21 CFR 876.5210. Orion Life Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent (kit))
Decision Date
June 28, 1990
Date Received
March 13, 1990
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enema Kit
Device Class
Class I
Regulation Number
876.5210
Review Panel
GU
Submission Type

This product code has been established in accordance with the may 20, 1997, guidance entitled, convenience kits interim regulatory guidance, found at www.fda.gov/cdrh/ode/convkit.html.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.