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FDA 510(k)

MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE

K-Number: K945102 · 1994-11-04

ApplicantAlm Surgical Equipment, Inc.
Decision Date1994-11-04
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Alm Surgical Equipment, Inc.. It received FDA 510(k) clearance on 1994-11-04 under 510(k) number K945102. 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 MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE?

MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1994-11-04. The listed applicant is Alm Surgical Equipment, Inc.. The 510(k) number is K945102.

When did MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE receive FDA 510(k) clearance?

MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE received FDA 510(k) clearance on 1994-11-04, under 510(k) number K945102.

Who is the listed applicant for MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE?

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

What is the FDA product code for MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE?

The FDA product code for MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCE is FFS.

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Other records listing Alm Surgical Equipment, 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.

K982063ALM PRISMALIX (PRX) SURGICAL LIGHTK961886DRAGER GEMINA WALL-MOUNTED WORKPLACEK961742DRAGER DVE 8080/81/82 WITH DVE 4002 OR DVE 4001 SERIES SYSTEMK942043DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032EK922409ALM ILLUMINATOR SERIES LIGHT SYSTEMK921297DRAGER DVE 4000 SERIES SYSTEM

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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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