The following data is part of a premarket notification filed by Abco Dealers, Inc. with the FDA for Bed Products.
Device ID | K850470 |
510k Number | K850470 |
Device Name: | BED PRODUCTS |
Classification | Restraint, Protective |
Applicant | ABCO DEALERS, INC. P.O. BOX 17587 6637 NORTH SIDNEY PLACE Milwaukee, WI 53217 |
Contact | Christine Nemeth |
Correspondent | Christine Nemeth ABCO DEALERS, INC. P.O. BOX 17587 6637 NORTH SIDNEY PLACE Milwaukee, WI 53217 |
Product Code | FMQ |
CFR Regulation Number | 880.6760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-01-28 |
Decision Date | 1985-04-01 |