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FDA 510(k)

HOT MINI 15 & HOT MINI 24

K-Number: K820359 · 1982-03-08

ApplicantHot Mini International, Inc.
Decision Date1982-03-08
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HOT MINI 15 & HOT MINI 24 is the device name listed in this FDA 510(k) record. The listed applicant is Hot Mini International, Inc.. It received FDA 510(k) clearance on 1982-03-08 under 510(k) number K820359. 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 HOT MINI 15 & HOT MINI 24?

HOT MINI 15 & HOT MINI 24 is a medical device that received FDA 510(k) clearance on 1982-03-08. The listed applicant is Hot Mini International, Inc.. The 510(k) number is K820359.

When did HOT MINI 15 & HOT MINI 24 receive FDA 510(k) clearance?

HOT MINI 15 & HOT MINI 24 received FDA 510(k) clearance on 1982-03-08, under 510(k) number K820359.

Who is the listed applicant for HOT MINI 15 & HOT MINI 24?

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

What is the FDA product code for HOT MINI 15 & HOT MINI 24?

The FDA product code for HOT MINI 15 & HOT MINI 24 is IMD.

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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