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)

HOT CYCLE, A CHEMICAL TYPE HOT PACK

K-Number: K802252 · 1980-10-03

ApplicantSignal West
Decision Date1980-10-03
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HOT CYCLE, A CHEMICAL TYPE HOT PACK is the device name listed in this FDA 510(k) record. The listed applicant is Signal West. It received FDA 510(k) clearance on 1980-10-03 under 510(k) number K802252. 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 CYCLE, A CHEMICAL TYPE HOT PACK?

HOT CYCLE, A CHEMICAL TYPE HOT PACK is a medical device that received FDA 510(k) clearance on 1980-10-03. The listed applicant is Signal West. The 510(k) number is K802252.

When did HOT CYCLE, A CHEMICAL TYPE HOT PACK receive FDA 510(k) clearance?

HOT CYCLE, A CHEMICAL TYPE HOT PACK received FDA 510(k) clearance on 1980-10-03, under 510(k) number K802252.

Who is the listed applicant for HOT CYCLE, A CHEMICAL TYPE HOT PACK?

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

What is the FDA product code for HOT CYCLE, A CHEMICAL TYPE HOT PACK?

The FDA product code for HOT CYCLE, A CHEMICAL TYPE HOT 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 Signal West 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.

↑