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FDA 510(k)

PES HOT/COLD COMPRESS

K-Number: K962038 · 1996-11-13

ApplicantPrinceton Electronic Systems, Inc.
Decision Date1996-11-13
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PES HOT/COLD COMPRESS is the device name listed in this FDA 510(k) record. The listed applicant is Princeton Electronic Systems, Inc.. It received FDA 510(k) clearance on 1996-11-13 under 510(k) number K962038. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PES HOT/COLD COMPRESS?

PES HOT/COLD COMPRESS is a medical device that received FDA 510(k) clearance on 1996-11-13. The listed applicant is Princeton Electronic Systems, Inc.. The 510(k) number is K962038.

When did PES HOT/COLD COMPRESS receive FDA 510(k) clearance?

PES HOT/COLD COMPRESS received FDA 510(k) clearance on 1996-11-13, under 510(k) number K962038.

Who is the listed applicant for PES HOT/COLD COMPRESS?

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

What is the FDA product code for PES HOT/COLD COMPRESS?

The FDA product code for PES HOT/COLD COMPRESS is IRT.

Related Clinical Trials

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Related Devices (Code: IRT)

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

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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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