The following data is part of a premarket notification filed by Deip Enterprises, Inc. with the FDA for Cervical Pillow.
Device ID | K830350 |
510k Number | K830350 |
Device Name: | CERVICAL PILLOW |
Classification | Orthosis, Cervical |
Applicant | DEIP ENTERPRISES, INC. 803 N. Front St. Suite 3 McHenry, IL 60050 |
Product Code | IQK |
CFR Regulation Number | 890.3490 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1983-02-03 |
Decision Date | 1983-03-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CERVICAL PILLOW 97234692 not registered Live/Pending |
He, Weijie 2022-01-24 |