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FDA 510(k)

SPIRIT SHIELD

K-Number: K931718 · 1993-09-20

Decision Date1993-09-20
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPIRIT SHIELD is the device name listed in this FDA 510(k) record. The listed applicant is Eaton Medical Corp.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K931718. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIRIT SHIELD?

SPIRIT SHIELD is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Eaton Medical Corp.. The 510(k) number is K931718.

When did SPIRIT SHIELD receive FDA 510(k) clearance?

SPIRIT SHIELD received FDA 510(k) clearance on 1993-09-20, under 510(k) number K931718.

Who is the listed applicant for SPIRIT SHIELD?

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

What is the FDA product code for SPIRIT SHIELD?

The FDA product code for SPIRIT SHIELD is HQY.

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 Eaton Medical 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.

Related Devices (Code: HQY)

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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