PMA P960042S013
- Device
- SPECTRANETICS LASER SHEATH (SLS)
- Applicant
- Spectranetics (Philips)
- PMA number
- P960042
- Supplement
- S013
- Product code
- MFA
- Decision date
- 2009-06-01
- Classification
- Device, Removal, Pacemaker Electrode, Percutaneous
- Generic name
- DEVICE, REMOVAL, PACEMAKER ELECTRODE, PERCUTANEOUS
- Approval order statement
- CHANGES TO THE IN-PROCESS ACCEPTANCE ACTIVITIES FOR THE LABELING AND BOXING PROCESS.
Current openFDA PMA Record#
- Device
- SPECTRANETICS LASER SHEATH (SLS)
- Applicant
- Spectranetics (Philips)
- PMA number
- P960042
- Supplement
- S013
- Product code
- MFA
- Generic name
- DEVICE, REMOVAL, PACEMAKER ELECTRODE, PERCUTANEOUS
- Decision date
- 2009-06-01
- Decision code
- OK30
- Date received
- 2009-05-05
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGES TO THE IN-PROCESS ACCEPTANCE ACTIVITIES FOR THE LABELING AND BOXING PROCESS.