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FDA 510(k)

TIGER BAND

K-Number: K844324 · 1984-12-03

Decision Date1984-12-03
Product CodeDZN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TIGER BAND is the device name listed in this FDA 510(k) record. The listed applicant is World Wide Outdoor Marketing. It received FDA 510(k) clearance on 1984-12-03 under 510(k) number K844324. The device is classified under product code DZN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGER BAND?

TIGER BAND is a medical device that received FDA 510(k) clearance on 1984-12-03. The listed applicant is World Wide Outdoor Marketing. The 510(k) number is K844324.

When did TIGER BAND receive FDA 510(k) clearance?

TIGER BAND received FDA 510(k) clearance on 1984-12-03, under 510(k) number K844324.

Who is the listed applicant for TIGER BAND?

The FDA 510(k) record lists World Wide Outdoor Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIGER BAND?

The FDA product code for TIGER BAND is DZN.

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.

Related Devices (Code: DZN)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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