The following data is part of a premarket notification filed by Caesarea Medical Electronics Ltd. with the FDA for Bodygaurd Pain Manager Infusion System.
Device ID | K061325 |
510k Number | K061325 |
Device Name: | BODYGAURD PAIN MANAGER INFUSION SYSTEM |
Classification | Pump, Infusion |
Applicant | CAESAREA MEDICAL ELECTRONICS LTD. 16 SHACHAM STREET CAESAREA INDUSTRIAL PARK Caesarea, IL 38900 |
Contact | Shlomi Dines |
Correspondent | Shlomi Dines CAESAREA MEDICAL ELECTRONICS LTD. 16 SHACHAM STREET CAESAREA INDUSTRIAL PARK Caesarea, IL 38900 |
Product Code | FRN |
CFR Regulation Number | 880.5725 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-05-11 |
Decision Date | 2006-08-24 |
Summary: | summary |