The following data is part of a premarket notification filed by Span-america Medical Systems, Inc. with the FDA for Pressure Guard Alternating Pressure Mattress.
Device ID | K954766 |
510k Number | K954766 |
Device Name: | PRESSURE GUARD ALTERNATING PRESSURE MATTRESS |
Classification | Mattress, Air Flotation, Alternating Pressure |
Applicant | SPAN-AMERICA MEDICAL SYSTEMS, INC. P.O. BOX 5231 Greenville, SC 29606 |
Contact | Wanda J Totton |
Correspondent | Wanda J Totton SPAN-AMERICA MEDICAL SYSTEMS, INC. P.O. BOX 5231 Greenville, SC 29606 |
Product Code | FNM |
CFR Regulation Number | 880.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-10-17 |
Decision Date | 1996-01-11 |