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FDA 510(k)

COLD-HOT PACK

K-Number: K820068 · 1982-01-28

Decision Date1982-01-28
Product CodeIME
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

COLD-HOT PACK is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Marketing Services Co., Inc.. It received FDA 510(k) clearance on 1982-01-28 under 510(k) number K820068. The device is classified under product code IME. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLD-HOT PACK?

COLD-HOT PACK is a medical device that received FDA 510(k) clearance on 1982-01-28. The listed applicant is Hospital Marketing Services Co., Inc.. The 510(k) number is K820068.

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

COLD-HOT PACK received FDA 510(k) clearance on 1982-01-28, under 510(k) number K820068.

Who is the listed applicant for COLD-HOT PACK?

The FDA 510(k) record lists Hospital Marketing Services Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLD-HOT PACK?

The FDA product code for COLD-HOT PACK is IME.

Related Devices (Code: IME)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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