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FDA 510(k)

ALM ILLUMINATOR SERIES LIGHT SYSTEM

K-Number: K922409 · 1993-01-12

ApplicantAlm Surgical Equipment, Inc.
Decision Date1993-01-12
Product CodeFSQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALM ILLUMINATOR SERIES LIGHT SYSTEM 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 1993-01-12 under 510(k) number K922409. The device is classified under product code FSQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALM ILLUMINATOR SERIES LIGHT SYSTEM?

ALM ILLUMINATOR SERIES LIGHT SYSTEM is a medical device that received FDA 510(k) clearance on 1993-01-12. The listed applicant is Alm Surgical Equipment, Inc.. The 510(k) number is K922409.

When did ALM ILLUMINATOR SERIES LIGHT SYSTEM receive FDA 510(k) clearance?

ALM ILLUMINATOR SERIES LIGHT SYSTEM received FDA 510(k) clearance on 1993-01-12, under 510(k) number K922409.

Who is the listed applicant for ALM ILLUMINATOR SERIES LIGHT SYSTEM?

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 ALM ILLUMINATOR SERIES LIGHT SYSTEM?

The FDA product code for ALM ILLUMINATOR SERIES LIGHT SYSTEM is FSQ.

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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 SYSTEMK945102MTA:ANGENIEUX STARPOINT XE XENON LIGHT SOURCEK942043DRAGER DVE 8000/1/2 SERIES SYST W/DVE 4002 AND 8032EK921297DRAGER DVE 4000 SERIES SYSTEM

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Related Devices (Code: FSQ)

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.

K930686MIDMARK SURGICAL LIGHTING SYSTEMSMidmark Corp.K932139LIGHTED INTUBATION STYLET W/REPLACEABLE SHAFTAaron Medical IndustriesK921848BFW WEHMERLITE IV-A FIBER OPTIC SURG. HEADLIGHTAlm Surgical Equipment, Inc.K803067SURG-FLEX 10 LIGHTMedical Products Development, Inc.K810019SURG-FLEX 15 SURGICAL LIGHTMedical Products Development, Inc.K810018SURG-FLEX 5 SURGICAL LIGHTMedical Products Development, 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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