The following data is part of a premarket notification filed by Geneva Laboratories, Inc. with the FDA for Gent-l-kare Cleansing Enema Set.
Device ID | K881218 |
510k Number | K881218 |
Device Name: | GENT-L-KARE CLEANSING ENEMA SET |
Classification | Enema Kit |
Applicant | GENEVA LABORATORIES, INC. P.O. BOX 444 Elkhorn, WI 53121 |
Contact | Gary L Swanson |
Correspondent | Gary L Swanson GENEVA LABORATORIES, INC. P.O. BOX 444 Elkhorn, WI 53121 |
Product Code | FCE |
CFR Regulation Number | 876.5210 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-03-22 |
Decision Date | 1988-07-28 |