PMA P980024S009
- Device
- PATHVYSION HER-2 DNA PROBE KIT
- Applicant
- Abbott Molecular, Inc.
- PMA number
- P980024
- Supplement
- S009
- Product code
- MVD
- Decision date
- 2012-12-26
- Classification
- System, Test, Her-2/neu, Nucleic Acid Or Serum
- Generic name
- SYSTEM, TEST, HER-2/NEU, NUCLEIC ACID OR SERUM
- Approval order statement
- QUALIFY THE GENEPREP INSTRUMENT, QUALIFY THE OVERHEAD MIXING SYSTEM AND VALIDATE THE MIXING PROCESS IN THE MANUFACTURE OF THE HYBRIDIZATION BUFFER, AND TRANSFER AN EXISTING IN-PROCESS TESTING OF LABELED DNA.
Current openFDA PMA Record#
- Device
- PATHVYSION HER-2 DNA PROBE KIT
- Applicant
- Abbott Molecular, Inc.
- PMA number
- P980024
- Supplement
- S009
- Product code
- MVD
- Generic name
- SYSTEM, TEST, HER-2/NEU, NUCLEIC ACID OR SERUM
- Decision date
- 2012-12-26
- Decision code
- OK30
- Date received
- 2012-11-15
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- QUALIFY THE GENEPREP INSTRUMENT, QUALIFY THE OVERHEAD MIXING SYSTEM AND VALIDATE THE MIXING PROCESS IN THE MANUFACTURE OF THE HYBRIDIZATION BUFFER, AND TRANSFER AN EXISTING IN-PROCESS TESTING OF LABELED DNA.