TL 20W/12/RS & TL 40W/12/RS
FDA 510(k) clearance K935840 · decided 1994-02-24
Clearance details
- K-number
- K935840
- Device name
- TL 20W/12/RS & TL 40W/12/RS
- Applicant
- Philips Lighting Co.
- Decision
- Substantially Equivalent
- Date received
- 1993-12-07
- Decision date
- 1994-02-24
- Days to decision
- 79 days
- Clearance type
- Traditional
- Product code
- FTC
- Device class
- 2
- Regulation number
- 878.4630
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Somerset, NJ, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
Recalls involving this device
No recalls on record reference this clearance.