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FDA 510(k)

FIBEROPTIC LIGHTSOURCES AND CARRIERS

K-Number: K933145 · 1993-09-07

Decision Date1993-09-07
Product CodeEQH
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FIBEROPTIC LIGHTSOURCES AND CARRIERS is the device name listed in this FDA 510(k) record. The listed applicant is Electro Fiberoptics Corp.. It received FDA 510(k) clearance on 1993-09-07 under 510(k) number K933145. The device is classified under product code EQH. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBEROPTIC LIGHTSOURCES AND CARRIERS?

FIBEROPTIC LIGHTSOURCES AND CARRIERS is a medical device that received FDA 510(k) clearance on 1993-09-07. The listed applicant is Electro Fiberoptics Corp.. The 510(k) number is K933145.

When did FIBEROPTIC LIGHTSOURCES AND CARRIERS receive FDA 510(k) clearance?

FIBEROPTIC LIGHTSOURCES AND CARRIERS received FDA 510(k) clearance on 1993-09-07, under 510(k) number K933145.

Who is the listed applicant for FIBEROPTIC LIGHTSOURCES AND CARRIERS?

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

What is the FDA product code for FIBEROPTIC LIGHTSOURCES AND CARRIERS?

The FDA product code for FIBEROPTIC LIGHTSOURCES AND CARRIERS is EQH.

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.

Other records listing Electro Fiberoptics 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.

Related Devices (Code: EQH)

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.

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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