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FDA 510(k)

UCEZ - STERILE LENS FOG REDUCTION DEVICE

K-Number: K905590 · 1991-05-10

ApplicantInman Liebelt Corp.
Decision Date1991-05-10
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

UCEZ - STERILE LENS FOG REDUCTION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Inman Liebelt Corp.. It received FDA 510(k) clearance on 1991-05-10 under 510(k) number K905590. 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 UCEZ - STERILE LENS FOG REDUCTION DEVICE?

UCEZ - STERILE LENS FOG REDUCTION DEVICE is a medical device that received FDA 510(k) clearance on 1991-05-10. The listed applicant is Inman Liebelt Corp.. The 510(k) number is K905590.

When did UCEZ - STERILE LENS FOG REDUCTION DEVICE receive FDA 510(k) clearance?

UCEZ - STERILE LENS FOG REDUCTION DEVICE received FDA 510(k) clearance on 1991-05-10, under 510(k) number K905590.

Who is the listed applicant for UCEZ - STERILE LENS FOG REDUCTION DEVICE?

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

What is the FDA product code for UCEZ - STERILE LENS FOG REDUCTION DEVICE?

The FDA product code for UCEZ - STERILE LENS FOG REDUCTION DEVICE is OCT.

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Other records listing Inman Liebelt 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.

K912211INTRAVASCULAR CATHETER SECURMENT DEVICEK912146URETERAL CATHETER HOLDERK905583ILC FORCEPS PADSK903611ILC LEG BAG HOLDERK903610O.R. TIP CLEANER

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

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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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