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)

TTU-100THERMAL THERAPY UNIT

K-Number: K913026 · 1991-12-13

Decision Date1991-12-13
Product CodeILO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TTU-100THERMAL THERAPY UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Danninger Medical Technology, Inc.. It received FDA 510(k) clearance on 1991-12-13 under 510(k) number K913026. 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 TTU-100THERMAL THERAPY UNIT?

TTU-100THERMAL THERAPY UNIT is a medical device that received FDA 510(k) clearance on 1991-12-13. The listed applicant is Danninger Medical Technology, Inc.. The 510(k) number is K913026.

When did TTU-100THERMAL THERAPY UNIT receive FDA 510(k) clearance?

TTU-100THERMAL THERAPY UNIT received FDA 510(k) clearance on 1991-12-13, under 510(k) number K913026.

Who is the listed applicant for TTU-100THERMAL THERAPY UNIT?

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

What is the FDA product code for TTU-100THERMAL THERAPY UNIT?

The FDA product code for TTU-100THERMAL THERAPY UNIT 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 Danninger Medical Technology, 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.

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.

↑