FDA 510(k)

1424 TUMISTORE

K-Number: K822914 · 1982-12-03

Decision Date1982-12-03

Product Code

DecisionSubstantially Equivalent

Device Summary

1424 TUMISTORE is the device name listed in this FDA 510(k) record. The listed applicant is Life-Tech Intl., Inc.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K822914. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 1424 TUMISTORE?

1424 TUMISTORE is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Life-Tech Intl., Inc.. The 510(k) number is K822914.

When did 1424 TUMISTORE receive FDA 510(k) clearance?

1424 TUMISTORE received FDA 510(k) clearance on 1982-12-03, under 510(k) number K822914.

Who is the listed applicant for 1424 TUMISTORE?

The FDA 510(k) record lists Life-Tech Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.

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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.