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FDA 510(k)

ILCO INFRARED LIGHT COAGULATOR

K-Number: K911600 · 1991-07-09

ApplicantHoll Meditronics, Inc.
Decision Date1991-07-09
Product CodeKNS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ILCO INFRARED LIGHT COAGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Holl Meditronics, Inc.. It received FDA 510(k) clearance on 1991-07-09 under 510(k) number K911600. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILCO INFRARED LIGHT COAGULATOR?

ILCO INFRARED LIGHT COAGULATOR is a medical device that received FDA 510(k) clearance on 1991-07-09. The listed applicant is Holl Meditronics, Inc.. The 510(k) number is K911600.

When did ILCO INFRARED LIGHT COAGULATOR receive FDA 510(k) clearance?

ILCO INFRARED LIGHT COAGULATOR received FDA 510(k) clearance on 1991-07-09, under 510(k) number K911600.

Who is the listed applicant for ILCO INFRARED LIGHT COAGULATOR?

The FDA 510(k) record lists Holl Meditronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ILCO INFRARED LIGHT COAGULATOR?

The FDA product code for ILCO INFRARED LIGHT COAGULATOR is KNS.

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Other records listing Holl Meditronics, Inc. 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.

K954171ARCO-MBC, ARCO MCK942095SONOCA IIIK893924MOTO-MED RF-II AND PICOK901737SONOCA II ULTRASONIC SURGICAL DEVICEK893926SONOCA ULTRASONIC SURGICAL SYSTEM

Related Devices (Code: KNS)

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.

K262460Rezum SystemBoston ScientificK260962SphincterotomeTaewoong Medical Co., Ltd.K252388Vanquish Water Vapor Ablation DeviceFrancis Medical, Inc.K252889Single Use 3-Lumen Needle Knife V (KD-V441M, KD-V451M)Olympus Medical Systems CorporationK250945Single Use Preloaded Sphincterotome V (Distal Wire Guided) (KD-VC600 Series); Single Use Sphincterotome V (Distal Wire Guided) (KD-VC400 Series); Single Use 3-Lumen Sphincterotome (KD-V Series); Disposable Triple Lumen Sphincterotome (KD Series)Olympus Medical Systems Corp.K250351Single Use Electrosurgical Knife (KD-612L, KD-612U); Single Use Electrosurgical Knife (KD-620UR); Single Use Electrosurgical Knife (KD-650L, KD-650U)Olympus Medical Systems Corporation

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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