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FDA 510(k)

PL EXAM LIGHT

K-Number: K860088 · 1986-01-24

ApplicantBurton Medical Products Corp.
Decision Date1986-01-24
Product CodeFTD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PL EXAM LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Burton Medical Products Corp.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K860088. 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 PL EXAM LIGHT?

PL EXAM LIGHT is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Burton Medical Products Corp.. The 510(k) number is K860088.

When did PL EXAM LIGHT receive FDA 510(k) clearance?

PL EXAM LIGHT received FDA 510(k) clearance on 1986-01-24, under 510(k) number K860088.

Who is the listed applicant for PL EXAM LIGHT?

The FDA 510(k) record lists Burton Medical Products Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PL EXAM LIGHT?

The FDA product code for PL EXAM LIGHT is FTD.

Related Clinical Trials

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.

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Other records listing Burton Medical Products Corp. 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.

K101537AIM 200, MAJOR SURGICAL LIGHTK042395OUTPATIENT III MINOR SURGERY LIGHTK000639VISIONARY 2000K963682GENIE' SINGLE CEILING AND DOUBLE CEILINGK961843GENIEK935102SATURN 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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