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FDA 510(k)

ANTI-SHOCK TROUSERS

K-Number: K873997 · 1987-12-15

Decision Date1987-12-15
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANTI-SHOCK TROUSERS is the device name listed in this FDA 510(k) record. The listed applicant is Simulaids, Inc.. It received FDA 510(k) clearance on 1987-12-15 under 510(k) number K873997. 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 ANTI-SHOCK TROUSERS?

ANTI-SHOCK TROUSERS is a medical device that received FDA 510(k) clearance on 1987-12-15. The listed applicant is Simulaids, Inc.. The 510(k) number is K873997.

When did ANTI-SHOCK TROUSERS receive FDA 510(k) clearance?

ANTI-SHOCK TROUSERS received FDA 510(k) clearance on 1987-12-15, under 510(k) number K873997.

Who is the listed applicant for ANTI-SHOCK TROUSERS?

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

What is the FDA product code for ANTI-SHOCK TROUSERS?

The FDA product code for ANTI-SHOCK TROUSERS is JOW.

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.

Related Devices (Code: JOW)

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

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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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