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FDA 510(k)

LUMINOUS 250 FIBEROPTIC ILLUMINATOR

K-Number: K921866 · 1992-07-08

ApplicantProgressive Dynamics, Inc.
Decision Date1992-07-08
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LUMINOUS 250 FIBEROPTIC 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 1992-07-08 under 510(k) number K921866. The device is classified under product code HBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUMINOUS 250 FIBEROPTIC ILLUMINATOR?

LUMINOUS 250 FIBEROPTIC ILLUMINATOR is a medical device that received FDA 510(k) clearance on 1992-07-08. The listed applicant is Progressive Dynamics, Inc.. The 510(k) number is K921866.

When did LUMINOUS 250 FIBEROPTIC ILLUMINATOR receive FDA 510(k) clearance?

LUMINOUS 250 FIBEROPTIC ILLUMINATOR received FDA 510(k) clearance on 1992-07-08, under 510(k) number K921866.

Who is the listed applicant for LUMINOUS 250 FIBEROPTIC 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 250 FIBEROPTIC ILLUMINATOR?

The FDA product code for LUMINOUS 250 FIBEROPTIC ILLUMINATOR is HBI.

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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 SYSTEMK944688LUMINOUS 150 DUAL LAMPFIBEROPTIC ILLUMINATORK933764LIFE-AIR 1000 PATIENT WARMING COVERK933593LUMINOUS 150 FIBEROPTIC ILLUMINATORK914382LIFE-AIR 1000 HYPOTHERMIC TREATMENT SYSTEMK914383LIFE-AIR 1000 PATIENT WARMING COVERS

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Related Devices (Code: HBI)

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.

K223183Light-Guide CablesOlympus Winter & Ibe GmbHK163185OptiLux LED IlluminatorIsolux, LLCK111342LIGHT GUIDE CABLESchott North AmericaK0529791125 XSB XENON FIBER-OPTIC LIGHT SOURCEIsolux, LLCK021931ENDOSCOPIC FIBEROPTIC CABLEGulf Medical FiberopticsK991208ENDOSCOPIC FIBEROPTIC CABLEIsolux America

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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