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FDA 510(k)

TI-COMFORTER

K-Number: K780927 · 1978-08-09

ApplicantAlden Products Co.
Decision Date1978-08-09
Product Code
DecisionSubstantially Equivalent

Device Summary

TI-COMFORTER is the device name listed in this FDA 510(k) record. The listed applicant is Alden Products Co.. It received FDA 510(k) clearance on 1978-08-09 under 510(k) number K780927. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TI-COMFORTER?

TI-COMFORTER is a medical device that received FDA 510(k) clearance on 1978-08-09. The listed applicant is Alden Products Co.. The 510(k) number is K780927.

When did TI-COMFORTER receive FDA 510(k) clearance?

TI-COMFORTER received FDA 510(k) clearance on 1978-08-09, under 510(k) number K780927.

Who is the listed applicant for TI-COMFORTER?

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

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.

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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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