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FDA 510(k)

FLEXIBLE LIQUID LIGHT GUIDE

K-Number: K834487 · 1984-02-21

ApplicantEndo Lase, Inc.
Decision Date1984-02-21
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FLEXIBLE LIQUID LIGHT GUIDE is the device name listed in this FDA 510(k) record. The listed applicant is Endo Lase, Inc.. It received FDA 510(k) clearance on 1984-02-21 under 510(k) number K834487. 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 FLEXIBLE LIQUID LIGHT GUIDE?

FLEXIBLE LIQUID LIGHT GUIDE is a medical device that received FDA 510(k) clearance on 1984-02-21. The listed applicant is Endo Lase, Inc.. The 510(k) number is K834487.

When did FLEXIBLE LIQUID LIGHT GUIDE receive FDA 510(k) clearance?

FLEXIBLE LIQUID LIGHT GUIDE received FDA 510(k) clearance on 1984-02-21, under 510(k) number K834487.

Who is the listed applicant for FLEXIBLE LIQUID LIGHT GUIDE?

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

What is the FDA product code for FLEXIBLE LIQUID LIGHT GUIDE?

The FDA product code for FLEXIBLE LIQUID LIGHT GUIDE is FFS.

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Other records listing Endo Lase, 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.

K853900ENDO-LASE CD40 FOR NEUROSURGERYK853878ENDO-LASE CD-100 CO2 LASER FOR NEUROSURGERYK855093MEDILAS 2 ND:YAG LASER SURGERY SYSTEMK853903ENDO-LASE CD40 CO2 FOR GYNECOLOGYK853876ENDO-LSE CD-100 CO2 LASER FOR GYNECOLOGYK853901ENDO-LASE CD 40 FOR DERMATOLOGY

View all 24 devices →

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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