The following data is part of a premarket notification filed by King Mfg. Co. with the FDA for Bed, Adjustable, Hospital, Folding, Field, W/o Mat.
Device ID | K885241 |
510k Number | K885241 |
Device Name: | BED, ADJUSTABLE, HOSPITAL, FOLDING, FIELD, W/O MAT |
Classification | Bed, Manual |
Applicant | KING MFG. CO. 2605 SUMMER AVE. P.O. BOX 3064 Memphis, TN 38112 |
Contact | Lawrence E Bright |
Correspondent | Lawrence E Bright KING MFG. CO. 2605 SUMMER AVE. P.O. BOX 3064 Memphis, TN 38112 |
Product Code | FNJ |
CFR Regulation Number | 880.5120 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-12-21 |
Decision Date | 1989-02-24 |