The following data is part of a premarket notification filed by Cook Ob/gyn with the FDA for Iumc Endometrial Sampler.
Device ID | K941298 |
510k Number | K941298 |
Device Name: | IUMC ENDOMETRIAL SAMPLER |
Classification | Brush, Endometrial |
Applicant | COOK OB/GYN 1100 WEST MORGAN ST. P.O. BOX 271 Spencer, IN 47460 |
Contact | Rick Lykins |
Correspondent | Rick Lykins COOK OB/GYN 1100 WEST MORGAN ST. P.O. BOX 271 Spencer, IN 47460 |
Product Code | HFE |
CFR Regulation Number | 884.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-03-17 |
Decision Date | 1995-02-13 |