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FDA 510(k)

KWICK KOOLER

K-Number: K771660 · 1977-11-07

ApplicantWorld Trade Assoc.
Decision Date1977-11-07
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

KWICK KOOLER is the device name listed in this FDA 510(k) record. The listed applicant is World Trade Assoc.. It received FDA 510(k) clearance on 1977-11-07 under 510(k) number K771660. 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 KWICK KOOLER?

KWICK KOOLER is a medical device that received FDA 510(k) clearance on 1977-11-07. The listed applicant is World Trade Assoc.. The 510(k) number is K771660.

When did KWICK KOOLER receive FDA 510(k) clearance?

KWICK KOOLER received FDA 510(k) clearance on 1977-11-07, under 510(k) number K771660.

Who is the listed applicant for KWICK KOOLER?

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

What is the FDA product code for KWICK KOOLER?

The FDA product code for KWICK KOOLER is IMD.

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Related Devices (Code: IMD)

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

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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