FDA 510(k)

VEST RESTRAINT

K-Number: K760868 · 1976-11-01

Decision Date1976-11-01

Product CodeKNW

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

VEST RESTRAINT is the device name listed in this FDA 510(k) record. The listed applicant is Orthopedic Equipment Co., Inc.. It received FDA 510(k) clearance on 1976-11-01 under 510(k) number K760868. The device is classified under product code KNW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VEST RESTRAINT?

VEST RESTRAINT is a medical device that received FDA 510(k) clearance on 1976-11-01. The listed applicant is Orthopedic Equipment Co., Inc.. The 510(k) number is K760868.

When did VEST RESTRAINT receive FDA 510(k) clearance?

VEST RESTRAINT received FDA 510(k) clearance on 1976-11-01, under 510(k) number K760868.

Who is the listed applicant for VEST RESTRAINT?

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

What is the FDA product code for VEST RESTRAINT?

The FDA product code for VEST RESTRAINT is KNW.

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Other records listing Orthopedic Equipment Co., Inc. as applicant

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Related Devices (Code: KNW)

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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.