The following data is part of a premarket notification filed by United Medical Equipment, Inc. with the FDA for Unit-matt 5000 Pressure Relief System.
Device ID | K962585 |
510k Number | K962585 |
Device Name: | UNIT-MATT 5000 PRESSURE RELIEF SYSTEM |
Classification | Mattress, Air Flotation, Alternating Pressure |
Applicant | UNITED MEDICAL EQUIPMENT, INC. 17 HENRY AVE. Park Ridge, NJ 07656 |
Contact | Arron Mei |
Correspondent | Arron Mei UNITED MEDICAL EQUIPMENT, INC. 17 HENRY AVE. Park Ridge, NJ 07656 |
Product Code | FNM |
CFR Regulation Number | 880.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-07-01 |
Decision Date | 1997-01-07 |