The following data is part of a premarket notification filed by Up Custom Design, Inc. with the FDA for U P Custom Design, Inc. Cot Equipment Carrier.
Device ID | K922816 |
510k Number | K922816 |
Device Name: | U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIER |
Classification | Stretcher, Hand-carried |
Applicant | UP CUSTOM DESIGN, INC. P.O. BOX 734 Menominee, MI 49859 |
Contact | Michael Settersten |
Correspondent | Michael Settersten UP CUSTOM DESIGN, INC. P.O. BOX 734 Menominee, MI 49859 |
Product Code | FPP |
CFR Regulation Number | 880.6900 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-06-11 |
Decision Date | 1993-07-13 |