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FDA 510(k)

THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202

K-Number: K011768 · 2001-08-03

ApplicantThermo-Electric Co.
Decision Date2001-08-03
Product CodeLSB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 is the device name listed in this FDA 510(k) record. The listed applicant is Thermo-Electric Co.. It received FDA 510(k) clearance on 2001-08-03 under 510(k) number K011768. The device is classified under product code LSB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202?

THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 is a medical device that received FDA 510(k) clearance on 2001-08-03. The listed applicant is Thermo-Electric Co.. The 510(k) number is K011768.

When did THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 receive FDA 510(k) clearance?

THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 received FDA 510(k) clearance on 2001-08-03, under 510(k) number K011768.

Who is the listed applicant for THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202?

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

What is the FDA product code for THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202?

The FDA product code for THERMO-THERAPY, MODELS TT-101, TT-201, AND TT-202 is LSB.

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Related Devices (Code: LSB)

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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