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FDA 510(k)

REDDY ILLUMINATOR

K-Number: K950960 · 1995-09-08

ApplicantLuxtec Corp.
Decision Date1995-09-08
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

REDDY ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Luxtec Corp.. It received FDA 510(k) clearance on 1995-09-08 under 510(k) number K950960. 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 REDDY ILLUMINATOR?

REDDY ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1995-09-08. The listed applicant is Luxtec Corp.. The 510(k) number is K950960.

When did REDDY ILLUMINATOR receive FDA 510(k) clearance?

REDDY ILLUMINATOR received FDA 510(k) clearance on 1995-09-08, under 510(k) number K950960.

Who is the listed applicant for REDDY ILLUMINATOR?

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

What is the FDA product code for REDDY ILLUMINATOR?

The FDA product code for REDDY ILLUMINATOR is FFS.

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Other records listing Luxtec 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.

K973193LUXSCOPEK970642TENOSCOPEK970562TENOSNAREK895248IMS5000 ILLUMINATED LOUPESK890716LUXTEC ACO SERIES 4000 LIGHT SOURCEK864387LUXTEC FIBEROPTIC CABLES

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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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