The following data is part of a premarket notification filed by Adel Medical Ltd. with the FDA for Sololift - Patient Transfer Stretcher.
Device ID | K871475 |
510k Number | K871475 |
Device Name: | SOLOLIFT - PATIENT TRANSFER STRETCHER |
Classification | Device, Transfer, Patient, Manual |
Applicant | ADEL MEDICAL LTD. 16700 S.E. 120TH AVE. P.O. BOX 542 Clackamas, OR 97015 |
Contact | David R Cole |
Correspondent | David R Cole ADEL MEDICAL LTD. 16700 S.E. 120TH AVE. P.O. BOX 542 Clackamas, OR 97015 |
Product Code | FMR |
CFR Regulation Number | 880.6785 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-04-14 |
Decision Date | 1987-05-11 |