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FDA 510(k)

LIBERTY HOT PACK AND LIBERTY KOLD PACK

K-Number: K902839 · 1990-07-25

ApplicantLiberty Ent.
Decision Date1990-07-25
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LIBERTY HOT PACK AND LIBERTY KOLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is Liberty Ent.. It received FDA 510(k) clearance on 1990-07-25 under 510(k) number K902839. The device is classified under product code IMD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIBERTY HOT PACK AND LIBERTY KOLD PACK?

LIBERTY HOT PACK AND LIBERTY KOLD PACK is a medical device that received FDA 510(k) clearance on 1990-07-25. The listed applicant is Liberty Ent.. The 510(k) number is K902839.

When did LIBERTY HOT PACK AND LIBERTY KOLD PACK receive FDA 510(k) clearance?

LIBERTY HOT PACK AND LIBERTY KOLD PACK received FDA 510(k) clearance on 1990-07-25, under 510(k) number K902839.

Who is the listed applicant for LIBERTY HOT PACK AND LIBERTY KOLD PACK?

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

What is the FDA product code for LIBERTY HOT PACK AND LIBERTY KOLD PACK?

The FDA product code for LIBERTY HOT PACK AND LIBERTY KOLD PACK is IMD.

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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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