The following data is part of a premarket notification filed by Manan Medical Products, Inc. with the FDA for Manan D Bag.
Device ID | K961986 |
510k Number | K961986 |
Device Name: | MANAN D BAG |
Classification | Bag, Bile Collecting |
Applicant | MANAN MEDICAL PRODUCTS, INC. 2200 CARLSON DR. Northbrook, IL 60062 |
Contact | Michael Plishka |
Correspondent | Michael Plishka MANAN MEDICAL PRODUCTS, INC. 2200 CARLSON DR. Northbrook, IL 60062 |
Product Code | EXF |
CFR Regulation Number | 876.5010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-05-21 |
Decision Date | 1997-03-13 |