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FDA 510(k)

SOLARTEC SOURCE 270, MODEL # 90123

K-Number: K983714 · 1998-12-23

ApplicantCogent Light Technologies, Inc.
Decision Date1998-12-23
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SOLARTEC SOURCE 270, MODEL # 90123 is the device name listed in this FDA 510(k) record. The listed applicant is Cogent Light Technologies, Inc.. It received FDA 510(k) clearance on 1998-12-23 under 510(k) number K983714. 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 SOLARTEC SOURCE 270, MODEL # 90123?

SOLARTEC SOURCE 270, MODEL # 90123 is a medical device that received FDA 510(k) clearance on 1998-12-23. The listed applicant is Cogent Light Technologies, Inc.. The 510(k) number is K983714.

When did SOLARTEC SOURCE 270, MODEL # 90123 receive FDA 510(k) clearance?

SOLARTEC SOURCE 270, MODEL # 90123 received FDA 510(k) clearance on 1998-12-23, under 510(k) number K983714.

Who is the listed applicant for SOLARTEC SOURCE 270, MODEL # 90123?

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

What is the FDA product code for SOLARTEC SOURCE 270, MODEL # 90123?

The FDA product code for SOLARTEC SOURCE 270, MODEL # 90123 is FFS.

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Other records listing Cogent Light Technologies, 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.

K001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159K971057COGENLIGHT TECHNOLOGIES XLS ILLUMINATOR SYSTEMK936048LIGHTWEAR(TM) SYST (LIGHTWEAR HEADLIGHT CLIP/HEADBAND)K933405COGENT LIGHT ILLUMINATOR 10010 XENON LIGHT SOURCE

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

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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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