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FDA 510(k)

MINOR SURGICAL LIGHT MODEL 180

K-Number: K841360 · 1984-04-24

ApplicantAmerican Sterilizer Co.
Decision Date1984-04-24
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINOR SURGICAL LIGHT MODEL 180 is the device name listed in this FDA 510(k) record. The listed applicant is American Sterilizer Co.. It received FDA 510(k) clearance on 1984-04-24 under 510(k) number K841360. 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 MINOR SURGICAL LIGHT MODEL 180?

MINOR SURGICAL LIGHT MODEL 180 is a medical device that received FDA 510(k) clearance on 1984-04-24. The listed applicant is American Sterilizer Co.. The 510(k) number is K841360.

When did MINOR SURGICAL LIGHT MODEL 180 receive FDA 510(k) clearance?

MINOR SURGICAL LIGHT MODEL 180 received FDA 510(k) clearance on 1984-04-24, under 510(k) number K841360.

Who is the listed applicant for MINOR SURGICAL LIGHT MODEL 180?

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

What is the FDA product code for MINOR SURGICAL LIGHT MODEL 180?

The FDA product code for MINOR SURGICAL LIGHT MODEL 180 is FTD.

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Other records listing American Sterilizer 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.

K943288AMSCO SQ240 SURGICAL LIGHTK931872THE EAGLE 3017 100% ETHYLENE OXIDE STERILIZERK922485CHEMDI-VHP CHEMICAL INDICATORK930493QUANTUM 3080 SURGICAL TABLEK905816ORTHOVISION TABLEK896674AMSCO QUANTUM LIGHT

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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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