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FDA 510(k)

FLOOR STANDING, OPERATING AND EXAMINING LIGHT

K-Number: K893813 · 1989-07-14

ApplicantAstralite Corp.
Decision Date1989-07-14
Product CodeFSS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLOOR STANDING, OPERATING AND EXAMINING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Astralite Corp.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893813. 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 STANDING, OPERATING AND EXAMINING LIGHT?

FLOOR STANDING, OPERATING AND EXAMINING LIGHT is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Astralite Corp.. The 510(k) number is K893813.

When did FLOOR STANDING, OPERATING AND EXAMINING LIGHT receive FDA 510(k) clearance?

FLOOR STANDING, OPERATING AND EXAMINING LIGHT received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893813.

Who is the listed applicant for FLOOR STANDING, OPERATING AND EXAMINING LIGHT?

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

What is the FDA product code for FLOOR STANDING, OPERATING AND EXAMINING LIGHT?

The FDA product code for FLOOR STANDING, OPERATING AND EXAMINING 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 Astralite 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.

K023004LFRE INDIRECT LARYNGOSCOPE

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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