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FDA 510(k)

CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE

K-Number: K942576 · 1994-07-05

ApplicantWhite Knight Healthcare
Decision Date1994-07-05
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is White Knight Healthcare. It received FDA 510(k) clearance on 1994-07-05 under 510(k) number K942576. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE?

CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE is a medical device that received FDA 510(k) clearance on 1994-07-05. The listed applicant is White Knight Healthcare. The 510(k) number is K942576.

When did CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE receive FDA 510(k) clearance?

CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE received FDA 510(k) clearance on 1994-07-05, under 510(k) number K942576.

Who is the listed applicant for CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE?

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

What is the FDA product code for CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE?

The FDA product code for CLEAR LENS ENDOSCOPIC FOG REDUCTION DEVICE is OCT.

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 White Knight Healthcare 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.

K951984WHITE KNIGHT SURGEON'S VESTK943809MONOGARD FACE SHIELDK942577SURGICAL TIP CLEANERK934969DUALGARD FACE SHIELD

Related Devices (Code: OCT)

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.

K251068KnoxFog Anti-fogging DeviceUv One Hygienics, Inc.K231822GOLFF Sterile Anti-Fog SolutionBatrik Medical Manufacturing, Inc.K221293E-Brik Visualization AssistantJdi Surgical, Inc.K190864Konix Anti-Fog SolutionTurkuaz Saglik Hizmetleri Medikal Temizlik Kimyasal UrunlerK181887AMD Anti-Fog SolutionAdvanced Medical Design Co., Ltd.K163257VitreOx Anti-fog SolutionSio2 Nanotech, LLC

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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