FDA 510(k)

FALL-SAFE VEST

K-Number: K841672 · 1984-07-03

Decision Date1984-07-03

Product CodeKMI

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

FALL-SAFE VEST is the device name listed in this FDA 510(k) record. The listed applicant is Fsm Corp.. It received FDA 510(k) clearance on 1984-07-03 under 510(k) number K841672. The device is classified under product code KMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FALL-SAFE VEST?

FALL-SAFE VEST is a medical device that received FDA 510(k) clearance on 1984-07-03. The listed applicant is Fsm Corp.. The 510(k) number is K841672.

When did FALL-SAFE VEST receive FDA 510(k) clearance?

FALL-SAFE VEST received FDA 510(k) clearance on 1984-07-03, under 510(k) number K841672.

Who is the listed applicant for FALL-SAFE VEST?

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

What is the FDA product code for FALL-SAFE VEST?

The FDA product code for FALL-SAFE VEST is KMI.

Other records listing Fsm Corp. 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.

K841671FALL-SAFE MONITOR

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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.