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FDA 510(k)

LATERAL FLARE INTERNAL COLLAR (LFIC)

K-Number: K971900 · 1997-12-18

ApplicantPro-Lfic, LLC
Decision Date1997-12-18
Product CodeLWJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LATERAL FLARE INTERNAL COLLAR (LFIC) is the device name listed in this FDA 510(k) record. The listed applicant is Pro-Lfic, LLC. It received FDA 510(k) clearance on 1997-12-18 under 510(k) number K971900. The device is classified under product code LWJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LATERAL FLARE INTERNAL COLLAR (LFIC)?

LATERAL FLARE INTERNAL COLLAR (LFIC) is a medical device that received FDA 510(k) clearance on 1997-12-18. The listed applicant is Pro-Lfic, LLC. The 510(k) number is K971900.

When did LATERAL FLARE INTERNAL COLLAR (LFIC) receive FDA 510(k) clearance?

LATERAL FLARE INTERNAL COLLAR (LFIC) received FDA 510(k) clearance on 1997-12-18, under 510(k) number K971900.

Who is the listed applicant for LATERAL FLARE INTERNAL COLLAR (LFIC)?

The FDA 510(k) record lists Pro-Lfic, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LATERAL FLARE INTERNAL COLLAR (LFIC)?

The FDA product code for LATERAL FLARE INTERNAL COLLAR (LFIC) is LWJ.

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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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