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FDA 510(k)

TRAPEZE FLOOR BASE

K-Number: K772261 · 1978-01-26

Decision Date1978-01-26
Product CodeFNJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TRAPEZE FLOOR BASE is the device name listed in this FDA 510(k) record. The listed applicant is Med Fusion Systems, Inc.. It received FDA 510(k) clearance on 1978-01-26 under 510(k) number K772261. The device is classified under product code FNJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRAPEZE FLOOR BASE?

TRAPEZE FLOOR BASE is a medical device that received FDA 510(k) clearance on 1978-01-26. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K772261.

When did TRAPEZE FLOOR BASE receive FDA 510(k) clearance?

TRAPEZE FLOOR BASE received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772261.

Who is the listed applicant for TRAPEZE FLOOR BASE?

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

What is the FDA product code for TRAPEZE FLOOR BASE?

The FDA product code for TRAPEZE FLOOR BASE is FNJ.

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.

Other records listing Med Fusion Systems, Inc. as applicant

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.

View all 22 devices →

Related Devices (Code: FNJ)

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

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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