Vista Ophthalmics Vitrectomy Probe
K-Number: K220030 · 2022-05-04
ApplicantVista Ophthalmics, LLC
Decision Date2022-05-04
Product CodeMLZ
Advisory CommitteeOP
DecisionSubstantially Equivalent
Device Summary
Vista Ophthalmics Vitrectomy Probe is a medical device manufactured by Vista Ophthalmics, LLC. It received FDA 510(k) clearance on 2022-05-04 under approval number K220030. The device is classified under product code MLZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Vista Ophthalmics Vitrectomy Probe?
Vista Ophthalmics Vitrectomy Probe is a medical device that received FDA 510(k) clearance on 2022-05-04. It is manufactured by Vista Ophthalmics, LLC. The 510(k) number is K220030.
When was Vista Ophthalmics Vitrectomy Probe approved by the FDA?
Vista Ophthalmics Vitrectomy Probe received FDA 510(k) clearance on 2022-05-04, under approval number K220030.
What company makes Vista Ophthalmics Vitrectomy Probe?
Vista Ophthalmics Vitrectomy Probe is manufactured by Vista Ophthalmics, LLC.
What is the FDA product code for Vista Ophthalmics Vitrectomy Probe?
The FDA product code for Vista Ophthalmics Vitrectomy Probe is MLZ.
Related Devices (Code: MLZ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.