SLS II AND GLIDELIGHT LASER SHEATH KITS
FDA premarket approval P960042/S052 · decided 2015-12-03
Approval details
- PMA number
- P960042
- Supplement
- S052
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- SLS II AND GLIDELIGHT LASER SHEATH KITS
- Generic name
- DEVICE, REMOVAL, PACEMAKER ELECTRODE, PERCUTANEOUS
- Applicant
- Spectranetics (Philips)
- Date received
- 2015-11-09
- Decision date
- 2015-12-03
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- MFA
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Colorado Springs, CO
- Statement
- A MODIFICATION TO THE ETHYLENE OXIDE (EO) STERILIZATION PROCESS.
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