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FDA 510(k)

SURGICAL LIGHT

K-Number: K823360 · 1982-12-03

ApplicantAmsco Co.
Decision Date1982-12-03
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGICAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Amsco Co.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823360. 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 SURGICAL LIGHT?

SURGICAL LIGHT is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Amsco Co.. The 510(k) number is K823360.

When did SURGICAL LIGHT receive FDA 510(k) clearance?

SURGICAL LIGHT received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823360.

Who is the listed applicant for SURGICAL LIGHT?

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

What is the FDA product code for SURGICAL LIGHT?

The FDA product code for SURGICAL LIGHT is FTD.

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Other records listing Amsco Co. 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.

K912471EAGLE 3000 SDSK854922AMSCO POLARIS SLK833187HALL OSTEONK832945EAGLE 2000 STERILIZER SERIES GAS/AERAK832187HALL OSCILLATORK832186HALL DRILL/REAMER

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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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