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FDA 510(k)

ZOEX ANTISHOCK TROUSERS

K-Number: K904267 · 1991-03-18

ApplicantZoex Corp.
Decision Date1991-03-18
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOEX ANTISHOCK TROUSERS is the device name listed in this FDA 510(k) record. The listed applicant is Zoex Corp.. It received FDA 510(k) clearance on 1991-03-18 under 510(k) number K904267. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZOEX ANTISHOCK TROUSERS?

ZOEX ANTISHOCK TROUSERS is a medical device that received FDA 510(k) clearance on 1991-03-18. The listed applicant is Zoex Corp.. The 510(k) number is K904267.

When did ZOEX ANTISHOCK TROUSERS receive FDA 510(k) clearance?

ZOEX ANTISHOCK TROUSERS received FDA 510(k) clearance on 1991-03-18, under 510(k) number K904267.

Who is the listed applicant for ZOEX ANTISHOCK TROUSERS?

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

What is the FDA product code for ZOEX ANTISHOCK TROUSERS?

The FDA product code for ZOEX ANTISHOCK TROUSERS is JOW.

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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.

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