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FDA 510(k)

STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS

K-Number: K854507 · 1986-02-07

ApplicantStorz Instrument Co.
Decision Date1986-02-07
Product CodeLXP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1986-02-07 under 510(k) number K854507. The device is classified under product code LXP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS?

STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS is a medical device that received FDA 510(k) clearance on 1986-02-07. The listed applicant is Storz Instrument Co.. The 510(k) number is K854507.

When did STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS receive FDA 510(k) clearance?

STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS received FDA 510(k) clearance on 1986-02-07, under 510(k) number K854507.

Who is the listed applicant for STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS?

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

What is the FDA product code for STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS?

The FDA product code for STORZ MVS 19 & 20 GAUGE SCLERAL PLUGS is LXP.

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Other records listing Storz Instrument Co. 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.

K980100STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACKK980488STORZ MILLENNIUM MICROSURGICL SYSTEM HIGH SPEED VITRECTOMY SYSTEMK972664STORZ MILLENNIUM VISCOUS FLUID SYSTEMK971439STORZ MICROFLOW AND STORZ STANDARD PHACOEMULSIFICATION NEEDLESK964743STORZ E8010 ERGOTEC/PREMIERE ADAPTORK960024STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH

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Related Devices (Code: LXP)

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.

K022186SCLERAL PLUGS, 19 AND 20 GAUGEMicrovision, Inc.K990872SCLERAL PLUGS, 19 AND 20 GAUGEOphthalmic Consultants, Inc.K945114VISITEC SCLERAL PLUGVisitec Co.K925671DISPOSABLE SCLERAL PLUGSO.R. Specialties, Inc.K880952PRISMA DISPOSABLE 19 AND 20 GAUGE SCLERAL PLUGSAdvanced Surgical Products, Inc.K880953ADVANCED SURGICAL 19 & 20 GAUGE DISP. SCLERAL PLUGAdvanced Surgical Products, Inc.

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.

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