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FDA 510(k)

T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP

K-Number: K073675 · 2008-05-08

Decision Date2008-05-08
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Gaymar Industries, Inc.. It received FDA 510(k) clearance on 2008-05-08 under 510(k) number K073675. The device is classified under product code ILO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP?

T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP is a medical device that received FDA 510(k) clearance on 2008-05-08. The listed applicant is Gaymar Industries, Inc.. The 510(k) number is K073675.

When did T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP receive FDA 510(k) clearance?

T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP received FDA 510(k) clearance on 2008-05-08, under 510(k) number K073675.

Who is the listed applicant for T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP?

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

What is the FDA product code for T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP?

The FDA product code for T-PUMP LOCALIZED TEMPERATURE THERAPY PUMP is ILO.

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 Gaymar Industries, Inc. 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.

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Related Devices (Code: ILO)

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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