PMA P970018S005
- Device
- PREPSTAIN SYSTEM
- Applicant
- Bd Diagnostic Systems
- PMA number
- P970018
- Supplement
- S005
- Product code
- MKQ
- Decision date
- 2003-10-27
- Generic name
- Processor, cervical cytology slide, automated
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED IN BURLINGTON, NORTH CAROLINA.
Current openFDA PMA Record#
- Device
- PREPSTAIN SYSTEM
- Applicant
- Bd Diagnostic Systems
- PMA number
- P970018
- Supplement
- S005
- Product code
- MKQ
- Generic name
- Processor, cervical cytology slide, automated
- Decision date
- 2003-10-27
- Decision code
- APPR
- Date received
- 2002-08-26
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- APPROVAL FOR A MANUFACTURING SITE LOCATED IN BURLINGTON, NORTH CAROLINA.