The following data is part of a premarket notification filed by Mpm Medical, Inc. with the FDA for Mpm Wet Dressing (saline).
Device ID | K926044 |
510k Number | K926044 |
Device Name: | MPM WET DRESSING (SALINE) |
Classification | Bandage, Liquid |
Applicant | MPM MEDICAL, INC. P.O. BOX 16598 Ft. Worth, TX 76162 -0598 |
Contact | Richard A Hamer |
Correspondent | Richard A Hamer MPM MEDICAL, INC. P.O. BOX 16598 Ft. Worth, TX 76162 -0598 |
Product Code | KMF |
CFR Regulation Number | 880.5090 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-12-01 |
Decision Date | 1993-04-08 |