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FDA 510(k)

NOVUS MULTIWAVELENGTH

K-Number: K932468 · 1993-09-22

ApplicantCoherent Medical Group
Decision Date1993-09-22
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NOVUS MULTIWAVELENGTH is the device name listed in this FDA 510(k) record. The listed applicant is Coherent Medical Group. It received FDA 510(k) clearance on 1993-09-22 under 510(k) number K932468. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NOVUS MULTIWAVELENGTH?

NOVUS MULTIWAVELENGTH is a medical device that received FDA 510(k) clearance on 1993-09-22. The listed applicant is Coherent Medical Group. The 510(k) number is K932468.

When did NOVUS MULTIWAVELENGTH receive FDA 510(k) clearance?

NOVUS MULTIWAVELENGTH received FDA 510(k) clearance on 1993-09-22, under 510(k) number K932468.

Who is the listed applicant for NOVUS MULTIWAVELENGTH?

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

What is the FDA product code for NOVUS MULTIWAVELENGTH?

The FDA product code for NOVUS MULTIWAVELENGTH is GEX. This falls under the Gastroenterology category.

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Other records listing Coherent Medical Group 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.

K963339COHERENT ULTRAPULSE CO2 SURGICAL LASERSK960032COHERENT VERSAPULSE AESTHETIC SURGICAL LASERSK932981COHERENT VERSAPULSE 2.1 HOLMIUM SURGICAL LASERSK923575COHERENT VERSAPLUSE 2.1 HOLMIUM SURG. LASERSK930981ACCULITE(TM) OTOPROBEK914136COHERENT VERSAPULSE(TM) 2.1XE/2.1L HOLMI SURG LASE

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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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