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FDA 510(k)

FLOOR LIGHT

K-Number: K882333 · 1988-06-23

ApplicantCommercial Products & Engineering Co.
Decision Date1988-06-23
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLOOR LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Commercial Products & Engineering Co.. It received FDA 510(k) clearance on 1988-06-23 under 510(k) number K882333. 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 FLOOR LIGHT?

FLOOR LIGHT is a medical device that received FDA 510(k) clearance on 1988-06-23. The listed applicant is Commercial Products & Engineering Co.. The 510(k) number is K882333.

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

FLOOR LIGHT received FDA 510(k) clearance on 1988-06-23, under 510(k) number K882333.

Who is the listed applicant for FLOOR LIGHT?

The FDA 510(k) record lists Commercial Products & Engineering Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FLOOR LIGHT?

The FDA product code for FLOOR LIGHT is FSS.

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 Commercial Products & Engineering 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.

K894891IRRIGATOR STANDK884542SIC 3999 FOLDING ADJUSTABLE HOSPITAL BEDK883463HOSPITAL BED CLOTHING CRADLEK873545PORTABLE FIELD DENTAL OPERATING & TREATMENT UNIT

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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