INSTANT HOT PACKS
K-Number: K963768 · 1996-11-25
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Device Summary
Frequently Asked Questions
What is the INSTANT HOT PACKS?
INSTANT HOT PACKS is a medical device that received FDA 510(k) clearance on 1996-11-25. The listed applicant is Kick Ice, Inc.. The 510(k) number is K963768.
When did INSTANT HOT PACKS receive FDA 510(k) clearance?
INSTANT HOT PACKS received FDA 510(k) clearance on 1996-11-25, under 510(k) number K963768.
Who is the listed applicant for INSTANT HOT PACKS?
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 HOT PACKS?
The FDA product code for INSTANT HOT PACKS 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.
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