The following data is part of a premarket notification filed by Span-america Medical Systems, Inc. with the FDA for Pressureguard: Selectcare.
Device ID | K960188 |
510k Number | K960188 |
Device Name: | PRESSUREGUARD: SELECTCARE |
Classification | Mattress, Air Flotation, Alternating Pressure |
Applicant | SPAN-AMERICA MEDICAL SYSTEMS, INC. 70 COMMERCE DR. P.O. BOX 5231 Greenville, SC 29615 |
Contact | Wanda J Totton |
Correspondent | Wanda J Totton SPAN-AMERICA MEDICAL SYSTEMS, INC. 70 COMMERCE DR. P.O. BOX 5231 Greenville, SC 29615 |
Product Code | FNM |
CFR Regulation Number | 880.5550 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-01-16 |
Decision Date | 1996-10-02 |
Summary: | summary |