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FDA 510(k)

SATURN LIGHT

K-Number: K935102 · 1994-06-27

ApplicantBurton Medical Products Corp.
Decision Date1994-06-27
Product CodeFTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SATURN 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 1994-06-27 under 510(k) number K935102. The device is classified under product code FTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SATURN LIGHT?

SATURN LIGHT is a medical device that received FDA 510(k) clearance on 1994-06-27. The listed applicant is Burton Medical Products Corp.. The 510(k) number is K935102.

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

SATURN LIGHT received FDA 510(k) clearance on 1994-06-27, under 510(k) number K935102.

Who is the listed applicant for SATURN 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 SATURN LIGHT?

The FDA product code for SATURN LIGHT is FTA.

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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 CEILINGK961843GENIEK942553GENESIS

View all 15 devices →

Related Devices (Code: FTA)

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.

K112133OASYS SURGICAL LIGHT CONTROLLEROasys HealthcareK102791EASYSUITE SURGICAL LIGHT CONTROL (ESLC)Image Stream Medical, Inc.K081698MAINSTREAM OR SURGICAL LIGHT CONTROL (MSLC)Image Stream Medical, Inc.K053321LIGHT GUARD LIGHT HANDLE AND LIGHT HANDLE COVERXodus Medical, Inc.K051505SCB/STERIS OR-LIGHT INTERFACE BOXKARL STORZ Endoscopy-America, Inc.K023704KSEA SCB ACC CONTROLKARL STORZ Endoscopy-America, 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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