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FDA 510(k)

LIGHT, SURGICAL, FLOOR STANDING

K-Number: K880540 · 1988-02-24

ApplicantFerguson Medical
Decision Date1988-02-24
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LIGHT, SURGICAL, FLOOR STANDING is the device name listed in this FDA 510(k) record. The listed applicant is Ferguson Medical. It received FDA 510(k) clearance on 1988-02-24 under 510(k) number K880540. The device is classified under product code FSS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT, SURGICAL, FLOOR STANDING?

LIGHT, SURGICAL, FLOOR STANDING is a medical device that received FDA 510(k) clearance on 1988-02-24. The listed applicant is Ferguson Medical. The 510(k) number is K880540.

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

LIGHT, SURGICAL, FLOOR STANDING received FDA 510(k) clearance on 1988-02-24, under 510(k) number K880540.

Who is the listed applicant for LIGHT, SURGICAL, FLOOR STANDING?

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

What is the FDA product code for LIGHT, SURGICAL, FLOOR STANDING?

The FDA product code for LIGHT, SURGICAL, FLOOR STANDING is FSS.

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Other records listing Ferguson Medical as applicant

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K033153DICOM THEATERK963794PUNCTURENEEDLEK962615TUMORLOCALIZER MRIK971813EMBLAK972217ORTHOPEDIC SCREW SYSTEMK972219ORTHOPEDIC PLATE SYSTEM

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Related Devices (Code: FSS)

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.

K091246ILED 3 MOBILE (I300M), TRULIGHT 5500 MOBILE (T500M), TRULIGHT 5300 MOBILE (T300M)Trumpf Medizin Systeme GmbH + Co. KGK003489NEXT GENERAL M20 SURGICAL LIGHT; NEXT GENERATION M16 MINOR SURGERY LIGHT; NEXT GENERATION SPOTLIGHT; NEXT GENERATION M8Medical Illumination International, Inc.K984124AESCULAP XENON LIGHT SOURCEAesculap, Inc.K981962CUDA PRODUCTS CORP. MODEL M300 (M-300) LIGHTSOURCECuda Products Co.K981821VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATORAngiolaz, Inc.K981469CERMAX300 LIGHTSOURCECuda Products Co.

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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