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FDA 510(k)

LABORIE FIBREOPTIC LIGHT CABLE

K-Number: K840605 · 1984-04-13

ApplicantTridak Division of Indicon, Inc.
Decision Date1984-04-13
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LABORIE FIBREOPTIC LIGHT CABLE is the device name listed in this FDA 510(k) record. The listed applicant is Tridak Division of Indicon, Inc.. It received FDA 510(k) clearance on 1984-04-13 under 510(k) number K840605. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABORIE FIBREOPTIC LIGHT CABLE?

LABORIE FIBREOPTIC LIGHT CABLE is a medical device that received FDA 510(k) clearance on 1984-04-13. The listed applicant is Tridak Division of Indicon, Inc.. The 510(k) number is K840605.

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

LABORIE FIBREOPTIC LIGHT CABLE received FDA 510(k) clearance on 1984-04-13, under 510(k) number K840605.

Who is the listed applicant for LABORIE FIBREOPTIC LIGHT CABLE?

The FDA 510(k) record lists Tridak Division of Indicon, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LABORIE FIBREOPTIC LIGHT CABLE?

The FDA product code for LABORIE FIBREOPTIC LIGHT CABLE is FFS.

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Other records listing Tridak Division of Indicon, 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.

K891007NONIMPLANTED ELECTRICAL CONTINENCE DEVICEK860744OPTHALMIC SURGICAL INSTRUMENTSK853059LABORIE FIBEROPTIC PRESSURE SENSOR & INTERFACEK852856LABORIE URODYNAMICS PROCESSORK851934CYTOLOGICAL CERVICAL SPATULA THE MULTI-SPATULAK842609R.L. MEDICAL TWIN LIGHT SOURCE

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Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, 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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