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FDA 510(k)

COLLIMATOR LIGHT SOURCE

K-Number: K924759 · 1992-12-09

ApplicantDenar Corp.
Decision Date1992-12-09
Product CodeIZT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

COLLIMATOR LIGHT SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Denar Corp.. It received FDA 510(k) clearance on 1992-12-09 under 510(k) number K924759. The device is classified under product code IZT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLLIMATOR LIGHT SOURCE?

COLLIMATOR LIGHT SOURCE is a medical device that received FDA 510(k) clearance on 1992-12-09. The listed applicant is Denar Corp.. The 510(k) number is K924759.

When did COLLIMATOR LIGHT SOURCE receive FDA 510(k) clearance?

COLLIMATOR LIGHT SOURCE received FDA 510(k) clearance on 1992-12-09, under 510(k) number K924759.

Who is the listed applicant for COLLIMATOR LIGHT SOURCE?

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

What is the FDA product code for COLLIMATOR LIGHT SOURCE?

The FDA product code for COLLIMATOR LIGHT SOURCE is IZT.

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Other records listing Denar 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.

K925705ACCURAD-200 SYSTEM & ACCURAD-300 PLUS SYSTEMK884845STERI-OSSK883373STERI-OSS HYDROXYAPATITE-COATED DENTAL IMPLANTK852802DENAR DENTAL IMPLANT

Official Source

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