Cleared Traditional

4K UHD LCD Monitor OEV321UH

K220069 · Olympus Medical Systems Corp. · General & Plastic Surgery
Mar 2022
Decision
58d
Days
Class 2
Risk

About This 510(k) Submission

K220069 is an FDA 510(k) clearance for the 4K UHD LCD Monitor OEV321UH, a Laparoscope, General & Plastic Surgery (Class II — Special Controls, product code GCJ), submitted by Olympus Medical Systems Corp. (Hachiochi-Shi, JP). The FDA issued a Cleared decision on March 9, 2022, 58 days after receiving the submission on January 10, 2022. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 876.1500.

Submission Details

510(k) Number K220069 FDA.gov
FDA Decision Cleared SESE
Date Received January 10, 2022
Decision Date March 09, 2022
Days to Decision 58 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code GCJ — Laparoscope, General & Plastic Surgery
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.1500
Definition Validated Reprocessing Instructions And Reprocessing Validation Data For This Device Type Must Be Included In A 510(k) Submission If The Device Is Reusable And Has Specific Design Features (please Refer To Table 2 Of 82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).

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