PHOTOCOAGULATOR LASER— 510(k) K780345
Substantially EquivalentCavitron Corp.
FDA 510(k) clearance K780345 for PHOTOCOAGULATOR LASER, Substantially Equivalent on 1978-05-09. Applicant: Cavitron Corp.. Device class: 2.
Clearance details
- Applicant
- Cavitron Corp.
- Product code
- Code HQB
- Device class
- Class 2
- Regulation
- 21 CFR 886.4690
- Advisory panel
- Ophthalmic
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code HQB
view all- K220263 — Vortex Surgical Laser Probes, Vortex Surgical Illuminated Laser Probes, Vortex Surgical Endoilluminators, Vortex Surgical Chandeliers
- K191846 — MAXReach Laser Probe
- K182646 — Vitreq disposable laser probes, light fibers and Chandelier
- K132614 — PEREGRINE CURVED ILLUMINATING LASER PROBE
- K122997 — 23GA CURVED ILLUMINATING LASER PROBE
More clearances from Cavitron Corp.
view allAdverse events under product code HQB
product code HQB- Other
- 2
- Total
- 2
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.