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FDA 510(k)

360 DEGREE FIXATION LIGHT

K-Number: K933739 · 1994-03-14

ApplicantVaritronics
Decision Date1994-03-14
Product CodeHPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

360 DEGREE FIXATION LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Varitronics. It received FDA 510(k) clearance on 1994-03-14 under 510(k) number K933739. The device is classified under product code HPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 360 DEGREE FIXATION LIGHT?

360 DEGREE FIXATION LIGHT is a medical device that received FDA 510(k) clearance on 1994-03-14. The listed applicant is Varitronics. The 510(k) number is K933739.

When did 360 DEGREE FIXATION LIGHT receive FDA 510(k) clearance?

360 DEGREE FIXATION LIGHT received FDA 510(k) clearance on 1994-03-14, under 510(k) number K933739.

Who is the listed applicant for 360 DEGREE FIXATION LIGHT?

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

What is the FDA product code for 360 DEGREE FIXATION LIGHT?

The FDA product code for 360 DEGREE FIXATION LIGHT is HPL.

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Related Devices (Code: HPL)

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.

K931731STORZ M824 FIXATION DEVICE FOR RETRACTIVE SURGERYStorz Instrument Co.K873914ANIMATED FIXATION TOYS (DISTANCE AND NEARPOINT)Richmond Products, Inc.K854383KERATOLUXCarl Zeiss, Inc.K801381FITE FIXATION TOY FOR OCULAR EXAMFite Engineering Corp.K800112AMBLYOPIA TRAINERLife-Tech Instruments, Inc.K781313VISION-STIMULATOR, CAMClement Clarke, Inc.

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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