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FDA 510(k)

UNIVERSAL LIGHT CABLE

K-Number: K894570 · 1989-10-13

ApplicantExpanded Optics, Inc.
Decision Date1989-10-13
Product CodeLDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL LIGHT CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Expanded Optics, Inc.. It received FDA 510(k) clearance on 1989-10-13 under 510(k) number K894570. The device is classified under product code LDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVERSAL LIGHT CABLE?

UNIVERSAL LIGHT CABLE is a medical device that received FDA 510(k) clearance on 1989-10-13. The listed applicant is Expanded Optics, Inc.. The 510(k) number is K894570.

When did UNIVERSAL LIGHT CABLE receive FDA 510(k) clearance?

UNIVERSAL LIGHT CABLE received FDA 510(k) clearance on 1989-10-13, under 510(k) number K894570.

Who is the listed applicant for UNIVERSAL LIGHT CABLE?

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

What is the FDA product code for UNIVERSAL LIGHT CABLE?

The FDA product code for UNIVERSAL LIGHT CABLE is LDQ.

Related Clinical Trials

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Other records listing Expanded Optics, 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.

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Related Devices (Code: LDQ)

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.

K993797EC-7701 FLUID WARMING CABINETEnthermics Medical Systems, Inc.K992258HOT SHOT FLUID WARMER IV FLUIDSInfra-Med Technologies, Inc.K981032PIV SYSTEMMedical Solutions, Inc.K973747CONTROLLED TEMPERATURE CABINET SYSTEMSmithK955661ACU-HALTGlederer & Co., Inc.K955776ACU-LABGlederer & 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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