YAG LASER 8000 - LOWER GI APPLICAT— 510(k) K840142
Substantially EquivalentCooper Lasersonics, Inc.
FDA 510(k) clearance K840142 for YAG LASER 8000 - LOWER GI APPLICAT, Substantially Equivalent on 1984-05-18. Applicant: Cooper Lasersonics, Inc.. Device class: 2.
Clearance details
- Applicant
- Cooper Lasersonics, Inc.
- Product code
- Code LNK
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code LNK
view allMore clearances from Cooper Lasersonics, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.