The following data is part of a premarket notification filed by Acme Medical Scale Co. with the FDA for Model 5002 Lift Weigh-scale.
Device ID | K922119 |
510k Number | K922119 |
Device Name: | MODEL 5002 LIFT WEIGH-SCALE |
Classification | Scale, Patient |
Applicant | ACME MEDICAL SCALE CO. 1801 ADAMS AVE. P.O. BOX 1922 San Leandro, CA 94577 |
Contact | Brett Good |
Correspondent | Brett Good ACME MEDICAL SCALE CO. 1801 ADAMS AVE. P.O. BOX 1922 San Leandro, CA 94577 |
Product Code | FRW |
CFR Regulation Number | 880.2720 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-05 |
Decision Date | 1993-02-03 |