FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PASCAL SYNTHESIS DELIVERY SYSTEM
K Number: K081744
·
Decision Sep 9, 2008
Classifications
1
FEI Numbers
476
Registration Numbers
479
Same Product Code
2793
Applicant Total
7
Review Days
82
Basic Information
- Device Name
- PASCAL SYNTHESIS DELIVERY SYSTEM
- K Number
- K081744
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- OPTIMEDICA CORPORATION
- Date Received
- June 19, 2008
- Decision Date
- September 9, 2008
- 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 OPTIMEDICA CORPORATION
| K Number | Device Name | ||
|---|---|---|---|
| K141079 | OPTIMEDICA CATALYS PRECISION LASER SYSTEM | Sep 11, 2014 | Substantially Equivalent |
| K121091 | CATALYS PRECISION LASER SYSTEM | Aug 28, 2012 | Substantially Equivalent |
| K113479 | OPTIMEDICA CATALYS PRECISION LASER SYSTEM | Dec 21, 2011 | Substantially Equivalent |
| K100019 | PASCAL STREAMLINE PHOTOCOAGULATOR | May 4, 2010 | Substantially Equivalent |
| K091666 | PASCAL PHOTOCOAGULATOR, PASCAL-US | Jul 15, 2009 | Substantially Equivalent |
| K062336 | OPTIMEDICA LASER INDIRECT OPHTHALMOSCOPE | Oct 19, 2006 | Substantially Equivalent |