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FDA 510(k)

MELIDE FIBEROPTIC LIGHT

K-Number: K051786 · 2005-08-15

ApplicantDesigns For Vision, Inc.
Decision Date2005-08-15
Product CodeFST
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MELIDE FIBEROPTIC LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Designs For Vision, Inc.. It received FDA 510(k) clearance on 2005-08-15 under 510(k) number K051786. The device is classified under product code FST. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MELIDE FIBEROPTIC LIGHT?

MELIDE FIBEROPTIC LIGHT is a medical device that received FDA 510(k) clearance on 2005-08-15. The listed applicant is Designs For Vision, Inc.. The 510(k) number is K051786.

When did MELIDE FIBEROPTIC LIGHT receive FDA 510(k) clearance?

MELIDE FIBEROPTIC LIGHT received FDA 510(k) clearance on 2005-08-15, under 510(k) number K051786.

Who is the listed applicant for MELIDE FIBEROPTIC LIGHT?

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

What is the FDA product code for MELIDE FIBEROPTIC LIGHT?

The FDA product code for MELIDE FIBEROPTIC LIGHT is FST.

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 Designs For Vision, 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.

K043530DVI CURING LIGHTK032283DESIGNS FOR VISION FIBEROPTIC LIGHTK013880DAYLITE XENON LIGHT SOURCESK801058ILLUMINATED SPECULUM

Related Devices (Code: FST)

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.

K200874TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal EndInnovasis, Inc.K122637LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999Stryker SpineK113697EIGR SURGICAL ILLUMINATION SYSTEMInvuity, Inc.K113330CABLECAPSensormedK102266ISOLED AC-POWERED LED HEADLIGHT SYSTEMIsolux, LLCK101496CABLECAP MODEL: WLF, STZ, ACMSensormed

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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