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FDA 510(k)

TRIPOD

K-Number: K060926 · 2006-05-19

ApplicantFreedom Designs, Inc.
Decision Date2006-05-19
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TRIPOD is the device name listed in this FDA 510(k) record. The listed applicant is Freedom Designs, Inc.. It received FDA 510(k) clearance on 2006-05-19 under 510(k) number K060926. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRIPOD?

TRIPOD is a medical device that received FDA 510(k) clearance on 2006-05-19. The listed applicant is Freedom Designs, Inc.. The 510(k) number is K060926.

When did TRIPOD receive FDA 510(k) clearance?

TRIPOD received FDA 510(k) clearance on 2006-05-19, under 510(k) number K060926.

Who is the listed applicant for TRIPOD?

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

What is the FDA product code for TRIPOD?

The FDA product code for TRIPOD is IOR.

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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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