Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

INSTANT COLD PACK

K-Number: K963666 · 1996-10-30

Decision Date1996-10-30
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INSTANT COLD PACK is the device name listed in this FDA 510(k) record. The listed applicant is Kick Ice, Inc.. It received FDA 510(k) clearance on 1996-10-30 under 510(k) number K963666. 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 INSTANT COLD PACK?

INSTANT COLD PACK is a medical device that received FDA 510(k) clearance on 1996-10-30. The listed applicant is Kick Ice, Inc.. The 510(k) number is K963666.

When did INSTANT COLD PACK receive FDA 510(k) clearance?

INSTANT COLD PACK received FDA 510(k) clearance on 1996-10-30, under 510(k) number K963666.

Who is the listed applicant for INSTANT COLD PACK?

The FDA 510(k) record lists Kick Ice, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTANT COLD PACK?

The FDA product code for INSTANT COLD PACK is IMD.

Related Clinical Trials

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.

Other records listing Kick Ice, Inc. as applicant

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.

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.

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.

↑