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FDA 510(k)

TUMBLE FORMS TRISTANDER

K-Number: K922965 · 1992-07-13

ApplicantTumble Forms
Decision Date1992-07-13
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TUMBLE FORMS TRISTANDER is the device name listed in this FDA 510(k) record. The listed applicant is Tumble Forms. It received FDA 510(k) clearance on 1992-07-13 under 510(k) number K922965. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUMBLE FORMS TRISTANDER?

TUMBLE FORMS TRISTANDER is a medical device that received FDA 510(k) clearance on 1992-07-13. The listed applicant is Tumble Forms. The 510(k) number is K922965.

When did TUMBLE FORMS TRISTANDER receive FDA 510(k) clearance?

TUMBLE FORMS TRISTANDER received FDA 510(k) clearance on 1992-07-13, under 510(k) number K922965.

Who is the listed applicant for TUMBLE FORMS TRISTANDER?

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

What is the FDA product code for TUMBLE FORMS TRISTANDER?

The FDA product code for TUMBLE FORMS TRISTANDER is INW.

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Related Devices (Code: INW)

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.

K944308JAMES LECKEY FREE STANDERJames Leckey DesignK944307JAMES LECKEY PRONE STANDERJames Leckey DesignK943974EURO TECH MARQUISE CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK943975EURO TECH PLATINUM CHIROPRACTIC TABLEProgressive Electrical TherapeuticsK940238TUMBLE FORMS JUNIOR TRISTANDERCamp Intl., Inc.K932233ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405Bailey Mfg. Co.

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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