PMA P990035S004
- Device
- SUNLIGHT OMNISENSE 7000S
- Applicant
- Beam-Med, Ltd.
- PMA number
- P990035
- Supplement
- S004
- Product code
- MUA
- Decision date
- 2001-11-30
- Generic name
- Bone sonometer
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AR RND NETWORKS LTD, JERUSALEM, ISREAL.
Current openFDA PMA Record#
- Device
- SUNLIGHT OMNISENSE 7000S
- Applicant
- Beam-Med, Ltd.
- PMA number
- P990035
- Supplement
- S004
- Product code
- MUA
- Generic name
- Bone sonometer
- Decision date
- 2001-11-30
- Decision code
- APPR
- Date received
- 2001-09-25
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED AR RND NETWORKS LTD, JERUSALEM, ISREAL.