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FDA 510(k)

TACAHE

K-Number: K052534 · 2006-01-27

Decision Date2006-01-27
Product CodeITI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TACAHE is the device name listed in this FDA 510(k) record. The listed applicant is Dalton Medical Corp.. It received FDA 510(k) clearance on 2006-01-27 under 510(k) number K052534. The device is classified under product code ITI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TACAHE?

TACAHE is a medical device that received FDA 510(k) clearance on 2006-01-27. The listed applicant is Dalton Medical Corp.. The 510(k) number is K052534.

When did TACAHE receive FDA 510(k) clearance?

TACAHE received FDA 510(k) clearance on 2006-01-27, under 510(k) number K052534.

Who is the listed applicant for TACAHE?

The FDA 510(k) record lists Dalton Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TACAHE?

The FDA product code for TACAHE is ITI.

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 Dalton Medical Corp. 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.

View all 7 devices →

Related Devices (Code: ITI)

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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