The following data is part of a premarket notification filed by London International Group, Inc. with the FDA for Regent Biogel Indicator Inner Surgical Glove.
Device ID | K980942 |
510k Number | K980942 |
Device Name: | REGENT BIOGEL INDICATOR INNER SURGICAL GLOVE |
Classification | Surgeon's Gloves |
Applicant | LONDON INTERNATIONAL GROUP, INC. 2926 COLUMBIA HIGHWAY P.O. BOX 8308 Dotham, AL 36303 |
Contact | Neil Anderson |
Correspondent | Neil Anderson LONDON INTERNATIONAL GROUP, INC. 2926 COLUMBIA HIGHWAY P.O. BOX 8308 Dotham, AL 36303 |
Product Code | KGO |
CFR Regulation Number | 878.4460 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-03-12 |
Decision Date | 1998-05-11 |