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FDA 510(k)

TELESCOPING BEDRAILS

K-Number: K772260 · 1978-01-26

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

Device Summary

TELESCOPING BEDRAILS 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 K772260. 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 TELESCOPING BEDRAILS?

TELESCOPING BEDRAILS 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 K772260.

When did TELESCOPING BEDRAILS receive FDA 510(k) clearance?

TELESCOPING BEDRAILS received FDA 510(k) clearance on 1978-01-26, under 510(k) number K772260.

Who is the listed applicant for TELESCOPING BEDRAILS?

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 TELESCOPING BEDRAILS?

The FDA product code for TELESCOPING BEDRAILS 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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