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FDA 510(k)

MODEL FEL5100 FLOOR LIGHT

K-Number: K895950 · 1989-10-31

ApplicantF.W. Lang Co.
Decision Date1989-10-31
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL FEL5100 FLOOR LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is F.W. Lang Co.. It received FDA 510(k) clearance on 1989-10-31 under 510(k) number K895950. 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 MODEL FEL5100 FLOOR LIGHT?

MODEL FEL5100 FLOOR LIGHT is a medical device that received FDA 510(k) clearance on 1989-10-31. The listed applicant is F.W. Lang Co.. The 510(k) number is K895950.

When did MODEL FEL5100 FLOOR LIGHT receive FDA 510(k) clearance?

MODEL FEL5100 FLOOR LIGHT received FDA 510(k) clearance on 1989-10-31, under 510(k) number K895950.

Who is the listed applicant for MODEL FEL5100 FLOOR LIGHT?

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

What is the FDA product code for MODEL FEL5100 FLOOR LIGHT?

The FDA product code for MODEL FEL5100 FLOOR LIGHT is FSS.

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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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