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FDA 510(k)

DEMETRON LC

K-Number: K014179 · 2002-02-04

ApplicantKerr Corp.
Decision Date2002-02-04
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEMETRON LC is the device name listed in this FDA 510(k) record. The listed applicant is Kerr Corp.. It received FDA 510(k) clearance on 2002-02-04 under 510(k) number K014179. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEMETRON LC?

DEMETRON LC is a medical device that received FDA 510(k) clearance on 2002-02-04. The listed applicant is Kerr Corp.. The 510(k) number is K014179.

When did DEMETRON LC receive FDA 510(k) clearance?

DEMETRON LC received FDA 510(k) clearance on 2002-02-04, under 510(k) number K014179.

Who is the listed applicant for DEMETRON LC?

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

What is the FDA product code for DEMETRON LC?

The FDA product code for DEMETRON LC is EBZ.

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Other records listing Kerr 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.

K091613TAKE 1K090292PREMISE MODIFIEDK081695DMC COMPOSITEK072622STANDOUT 2K042888DEMETRON IDS CURING LIGHTK031484STAND OUT

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Related Devices (Code: EBZ)

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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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.

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