The following data is part of a premarket notification filed by Kinetic Concepts, Inc. with the FDA for Home Care Bead Bed.
Device ID | K972176 |
510k Number | K972176 |
Device Name: | HOME CARE BEAD BED |
Classification | Bed, Air Fluidized |
Applicant | KINETIC CONCEPTS, INC. P.O. BOX 659508 San Antonio, TX 78265 -9508 |
Contact | William H Quirk |
Correspondent | William H Quirk KINETIC CONCEPTS, INC. P.O. BOX 659508 San Antonio, TX 78265 -9508 |
Product Code | INX |
CFR Regulation Number | 890.5160 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-06-09 |
Decision Date | 1998-01-16 |
Summary: | summary |