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FDA 510(k)

I.C.E. BOX

K-Number: K821920 · 1982-08-31

ApplicantLhs Industries
Decision Date1982-08-31
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

I.C.E. BOX is the device name listed in this FDA 510(k) record. The listed applicant is Lhs Industries. It received FDA 510(k) clearance on 1982-08-31 under 510(k) number K821920. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.C.E. BOX?

I.C.E. BOX is a medical device that received FDA 510(k) clearance on 1982-08-31. The listed applicant is Lhs Industries. The 510(k) number is K821920.

When did I.C.E. BOX receive FDA 510(k) clearance?

I.C.E. BOX received FDA 510(k) clearance on 1982-08-31, under 510(k) number K821920.

Who is the listed applicant for I.C.E. BOX?

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

What is the FDA product code for I.C.E. BOX?

The FDA product code for I.C.E. BOX is IRP.

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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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