The following data is part of a premarket notification filed by Century Manufacturing Co. with the FDA for Century Scale.
Device ID | K844872 |
510k Number | K844872 |
Device Name: | CENTURY SCALE |
Classification | Lift, Patient, Ac-powered |
Applicant | CENTURY MANUFACTURING CO. 1201 LINCOLN MALL SUITE 102 Lincoln, 68508 |
Contact | Rick D Lange |
Correspondent | Rick D Lange CENTURY MANUFACTURING CO. 1201 LINCOLN MALL SUITE 102 Lincoln, 68508 |
Product Code | FNG |
CFR Regulation Number | 880.5500 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1984-12-17 |
Decision Date | 1985-02-08 |