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FDA 510(k)

FLARE,FILE, FILL

K-Number: K981234 · 1998-06-05

ApplicantLone Star Technologies
Decision Date1998-06-05
Product CodeEJB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FLARE,FILE, FILL is the device name listed in this FDA 510(k) record. The listed applicant is Lone Star Technologies. It received FDA 510(k) clearance on 1998-06-05 under 510(k) number K981234. The device is classified under product code EJB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLARE,FILE, FILL?

FLARE,FILE, FILL is a medical device that received FDA 510(k) clearance on 1998-06-05. The listed applicant is Lone Star Technologies. The 510(k) number is K981234.

When did FLARE,FILE, FILL receive FDA 510(k) clearance?

FLARE,FILE, FILL received FDA 510(k) clearance on 1998-06-05, under 510(k) number K981234.

Who is the listed applicant for FLARE,FILE, FILL?

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

What is the FDA product code for FLARE,FILE, FILL?

The FDA product code for FLARE,FILE, FILL is EJB.

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Other records listing Lone Star Technologies 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.

K980968LONE STAR IMPRESSION SYSTEMS

Related Devices (Code: EJB)

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

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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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