The following data is part of a premarket notification filed by Mego Afek with the FDA for Pbs Model 701a Compression Therapy Device.
Device ID | K060220 |
510k Number | K060220 |
Device Name: | PBS MODEL 701A COMPRESSION THERAPY DEVICE |
Classification | Sleeve, Limb, Compressible |
Applicant | MEGO AFEK BEIT HAPA'AMON (BOX 124) 20 HATA'AS ST., Kfar Saba, IL 44425 |
Contact | Ahava M Stein |
Correspondent | Ahava M Stein MEGO AFEK BEIT HAPA'AMON (BOX 124) 20 HATA'AS ST., Kfar Saba, IL 44425 |
Product Code | JOW |
CFR Regulation Number | 870.5800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-01-30 |
Decision Date | 2006-02-09 |
Summary: | summary |