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FDA 510(k)

QUICK-CAST IMMOBILIZER

K-Number: K932507 · 1994-02-23

ApplicantLandec Corp.
Decision Date1994-02-23
Product CodeLGF
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

QUICK-CAST IMMOBILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Landec Corp.. It received FDA 510(k) clearance on 1994-02-23 under 510(k) number K932507. The device is classified under product code LGF. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the QUICK-CAST IMMOBILIZER?

QUICK-CAST IMMOBILIZER is a medical device that received FDA 510(k) clearance on 1994-02-23. The listed applicant is Landec Corp.. The 510(k) number is K932507.

When did QUICK-CAST IMMOBILIZER receive FDA 510(k) clearance?

QUICK-CAST IMMOBILIZER received FDA 510(k) clearance on 1994-02-23, under 510(k) number K932507.

Who is the listed applicant for QUICK-CAST IMMOBILIZER?

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

What is the FDA product code for QUICK-CAST IMMOBILIZER?

The FDA product code for QUICK-CAST IMMOBILIZER is LGF.

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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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