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FDA 510(k)

EAGLE MEDICAL ANTI-FOG KIT

K-Number: K933618 · 1994-03-07

Decision Date1994-03-07
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EAGLE MEDICAL ANTI-FOG KIT is the device name listed in this FDA 510(k) record. The listed applicant is Eagle Medical Intl.. It received FDA 510(k) clearance on 1994-03-07 under 510(k) number K933618. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EAGLE MEDICAL ANTI-FOG KIT?

EAGLE MEDICAL ANTI-FOG KIT is a medical device that received FDA 510(k) clearance on 1994-03-07. The listed applicant is Eagle Medical Intl.. The 510(k) number is K933618.

When did EAGLE MEDICAL ANTI-FOG KIT receive FDA 510(k) clearance?

EAGLE MEDICAL ANTI-FOG KIT received FDA 510(k) clearance on 1994-03-07, under 510(k) number K933618.

Who is the listed applicant for EAGLE MEDICAL ANTI-FOG KIT?

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

What is the FDA product code for EAGLE MEDICAL ANTI-FOG KIT?

The FDA product code for EAGLE MEDICAL ANTI-FOG KIT is OCT.

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: OCT)

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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