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FDA 510(k)

ALM SURGICAL LAMPS

K-Number: K882613 · 1988-07-18

ApplicantAlm Surgical Equipment, Inc.
Decision Date1988-07-18
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ALM SURGICAL LAMPS 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 1988-07-18 under 510(k) number K882613. The device is classified under product code FTD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALM SURGICAL LAMPS?

ALM SURGICAL LAMPS is a medical device that received FDA 510(k) clearance on 1988-07-18. The listed applicant is Alm Surgical Equipment, Inc.. The 510(k) number is K882613.

When did ALM SURGICAL LAMPS receive FDA 510(k) clearance?

ALM SURGICAL LAMPS received FDA 510(k) clearance on 1988-07-18, under 510(k) number K882613.

Who is the listed applicant for ALM SURGICAL LAMPS?

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 SURGICAL LAMPS?

The FDA product code for ALM SURGICAL LAMPS is FTD.

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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 8032EK922409ALM ILLUMINATOR SERIES LIGHT SYSTEM

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Related Devices (Code: FTD)

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.

K133425SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHTEngineered Medical Solutions Co., LLCK130513VOLISTA 400; VOLISTA 600Maquet S.A.S.K123776POLARIS 100/200Drager Medical GmbHK111020ATRICURE DISSECTORAtriCure, Inc.K100234HM-LAMP IIHillusa, Inc.K100884STRYKER KNIFELIGHTHowmedica Osteonics Corp.

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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