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FDA 510(k)

INSTANT HOT & COLD PACKS

K-Number: K790993 · 1979-09-07

Decision Date1979-09-07
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INSTANT HOT & COLD PACKS is the device name listed in this FDA 510(k) record. The listed applicant is Chase Mfg. Co.. It received FDA 510(k) clearance on 1979-09-07 under 510(k) number K790993. 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 HOT & COLD PACKS?

INSTANT HOT & COLD PACKS is a medical device that received FDA 510(k) clearance on 1979-09-07. The listed applicant is Chase Mfg. Co.. The 510(k) number is K790993.

When did INSTANT HOT & COLD PACKS receive FDA 510(k) clearance?

INSTANT HOT & COLD PACKS received FDA 510(k) clearance on 1979-09-07, under 510(k) number K790993.

Who is the listed applicant for INSTANT HOT & COLD PACKS?

The FDA 510(k) record lists Chase Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTANT HOT & COLD PACKS?

The FDA product code for INSTANT HOT & COLD 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 Chase Mfg. Co. 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.

View all 10 devices →

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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