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FDA 510(k)

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS

K-Number: K873364 · 1987-11-17

ApplicantHypertherm Technologies, Inc.
Decision Date1987-11-17
Product CodeIMD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS is the device name listed in this FDA 510(k) record. The listed applicant is Hypertherm Technologies, Inc.. It received FDA 510(k) clearance on 1987-11-17 under 510(k) number K873364. 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 HYPERTHERM TECHNOLOGIES' HEAT COMPRESS?

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS is a medical device that received FDA 510(k) clearance on 1987-11-17. The listed applicant is Hypertherm Technologies, Inc.. The 510(k) number is K873364.

When did HYPERTHERM TECHNOLOGIES' HEAT COMPRESS receive FDA 510(k) clearance?

HYPERTHERM TECHNOLOGIES' HEAT COMPRESS received FDA 510(k) clearance on 1987-11-17, under 510(k) number K873364.

Who is the listed applicant for HYPERTHERM TECHNOLOGIES' HEAT COMPRESS?

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

What is the FDA product code for HYPERTHERM TECHNOLOGIES' HEAT COMPRESS?

The FDA product code for HYPERTHERM TECHNOLOGIES' HEAT COMPRESS is IMD.

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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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