Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL

K-Number: K920167 · 1992-03-23

ApplicantNextec Corp.
Decision Date1992-03-23
Product CodeHBI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL is the device name listed in this FDA 510(k) record. The listed applicant is Nextec Corp.. It received FDA 510(k) clearance on 1992-03-23 under 510(k) number K920167. The device is classified under product code HBI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL?

NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL is a medical device that received FDA 510(k) clearance on 1992-03-23. The listed applicant is Nextec Corp.. The 510(k) number is K920167.

When did NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL receive FDA 510(k) clearance?

NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL received FDA 510(k) clearance on 1992-03-23, under 510(k) number K920167.

Who is the listed applicant for NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL?

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

What is the FDA product code for NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL?

The FDA product code for NEXTEC FIBEROPTIC ILLUMINAT 150 WATT/HALO/3500 KEL is HBI.

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.

Other records listing Nextec 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.

Related Devices (Code: HBI)

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.

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.

↑