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FDA 510(k)

DEVMED LENS WASH SHEATH

K-Number: K925669 · 1993-02-23

ApplicantDevmed Corp.
Decision Date1993-02-23
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DEVMED LENS WASH SHEATH is the device name listed in this FDA 510(k) record. The listed applicant is Devmed Corp.. It received FDA 510(k) clearance on 1993-02-23 under 510(k) number K925669. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVMED LENS WASH SHEATH?

DEVMED LENS WASH SHEATH is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is Devmed Corp.. The 510(k) number is K925669.

When did DEVMED LENS WASH SHEATH receive FDA 510(k) clearance?

DEVMED LENS WASH SHEATH received FDA 510(k) clearance on 1993-02-23, under 510(k) number K925669.

Who is the listed applicant for DEVMED LENS WASH SHEATH?

The FDA 510(k) record lists Devmed Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEVMED LENS WASH SHEATH?

The FDA product code for DEVMED LENS WASH SHEATH is GCJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Devmed Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K972152DEVMED STEPPING AND STABILIZING SYSTEMK933416DEVMED LAP WASH REUSABLE ENDOSCOPIC LENS WASH SHEATH

Related Devices (Code: GCJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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