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FDA 510(k)

ARMOR-KOT SURGICAL INSTRUMENTS

K-Number: K771680 · 1977-11-28

ApplicantStorz Instrument Co.
Decision Date1977-11-28
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARMOR-KOT SURGICAL INSTRUMENTS 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 1977-11-28 under 510(k) number K771680. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARMOR-KOT SURGICAL INSTRUMENTS?

ARMOR-KOT SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Storz Instrument Co.. The 510(k) number is K771680.

When did ARMOR-KOT SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

ARMOR-KOT SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1977-11-28, under 510(k) number K771680.

Who is the listed applicant for ARMOR-KOT SURGICAL INSTRUMENTS?

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 ARMOR-KOT SURGICAL INSTRUMENTS?

The FDA product code for ARMOR-KOT SURGICAL INSTRUMENTS is FSM.

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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: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., 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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