Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Water Container (MAJ-901); Water Container (MAJ-902)

K-Number: K242357 · 2024-10-07

ApplicantOlympus Medical Systems Corporation
Decision Date2024-10-07
Product CodeOCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Water Container (MAJ-901); Water Container (MAJ-902) is a medical device manufactured by Olympus Medical Systems Corporation. It received FDA 510(k) clearance on 2024-10-07 under approval number K242357. The device is classified under product code OCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Water Container (MAJ-901); Water Container (MAJ-902)?

Water Container (MAJ-901); Water Container (MAJ-902) is a medical device that received FDA 510(k) clearance on 2024-10-07. It is manufactured by Olympus Medical Systems Corporation. The 510(k) number is K242357.

When was Water Container (MAJ-901); Water Container (MAJ-902) approved by the FDA?

Water Container (MAJ-901); Water Container (MAJ-902) received FDA 510(k) clearance on 2024-10-07, under approval number K242357.

What company makes Water Container (MAJ-901); Water Container (MAJ-902)?

Water Container (MAJ-901); Water Container (MAJ-902) is manufactured by Olympus Medical Systems Corporation.

What is the FDA product code for Water Container (MAJ-901); Water Container (MAJ-902)?

The FDA product code for Water Container (MAJ-901); Water Container (MAJ-902) is OCX.

Other Devices by Olympus Medical Systems Corporation

K211838Ultrasonic Bipolar Generator USG-410 with accessories K221557Visera Hysterovideoscope Olympus HYF Type V K222861EVIS XI Video System Center Olympus CV-1500, Bronchovideoscope Olympus BF-H1100, Bronchovideoscope Olympus BF-1TH1100 K222584EVIS X1 VIDEO SYSTEM CENTER OLYMPUS CV-1500, COLONOVIDEOSCOPE OLYMPUS CF-HQ1100DL/I, GASTROINTESTINAL VIDEOSCOPE OLYMPUS GIF-1100 K221683CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-V2R), CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VH) and CYSTO-NEPHRO VIDEOSCOPE (OLYMPUS CYF-VHR) K241371VISERA S VIDEO SYSTEM CENTER OLYMPUS OTV-S500 (OLYMPUS OTV-S500)

View all 31 devices →

Related Devices (Code: OCX)

K161167Seal Single-Use Biopsy ValveEndochoice, Inc. K152278ENDOFLOW II - Irrigation, Warming and Suction SystemPromepla Sam K182444ERBEFLO Olympus Scope Port ConnectorErbe USA, Inc. K182275Seal Single Use Biopsy ValveBoston Scientific Corporation K181509Endorate Valve SetsSmartdata Suzhou Co., Ltd. K173758Disposable Biopsy ValveZhejiang Chuangxiang Medical Technology Co., Ltd.

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.

↑