FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
REVLITE Q-SWITCHED ND: YAG LASER SYSTEM WITH NADPIECE ADAPTOR
K Number: K103118
·
Decision Nov 19, 2010
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
5
Review Days
29
Basic Information
- Device Name
- REVLITE Q-SWITCHED ND: YAG LASER SYSTEM WITH NADPIECE ADAPTOR
- K Number
- K103118
- Device Class
- FDA class 2
- Clearance Type
- Special
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- HOYA PHOTONICS, INC.
- Date Received
- October 21, 2010
- Decision Date
- November 19, 2010
- Product Code
- GEX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | FDA class 2 | General, Plastic Surgery |
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Other Clearances by HOYA PHOTONICS, INC.
| K Number | Device Name | ||
|---|---|---|---|
| K050696 | MEDLITE C1 Q-SWITCHED ND:YAG LASER | Jun 17, 2005 | Substantially Equivalent |
| K050274 | DIODENT II DENTAL LASER SYSTEM | Apr 29, 2005 | Substantially Equivalent |
| K041721 | LVI AESTHETIC LASER | Aug 5, 2004 | Substantially Equivalent |
| K032797 | DELIGHT DENTAL ER: YAG LASER SYSTEM | Apr 5, 2004 | Substantially Equivalent |