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FDA 510(k)

LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR

K-Number: K944688 · 1994-11-01

ApplicantProgressive Dynamics, Inc.
Decision Date1994-11-01
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Progressive Dynamics, Inc.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K944688. 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 LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR?

LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Progressive Dynamics, Inc.. The 510(k) number is K944688.

When did LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR receive FDA 510(k) clearance?

LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR received FDA 510(k) clearance on 1994-11-01, under 510(k) number K944688.

Who is the listed applicant for LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR?

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

What is the FDA product code for LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR?

The FDA product code for LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATOR is FFS.

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Other records listing Progressive Dynamics, 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.

K952329LIFE-AIR 1000 HYPOTHERMIC THERAPY SYSTEMK933764LIFE-AIR 1000 PATIENT WARMING COVERK933593LUMINOUS 150 FIBEROPTIC ILLUMINATORK921866LUMINOUS 250 FIBEROPTIC ILLUMINATORK914382LIFE-AIR 1000 HYPOTHERMIC TREATMENT SYSTEMK914383LIFE-AIR 1000 PATIENT WARMING COVERS

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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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