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FDA 510(k)

PINWORM EGG COLLECTOR

K-Number: K950096 · 1995-04-05

ApplicantEvergreen Industries, Inc.
Decision Date1995-04-05
Product CodeLIO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PINWORM EGG COLLECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Evergreen Industries, Inc.. It received FDA 510(k) clearance on 1995-04-05 under 510(k) number K950096. The device is classified under product code LIO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PINWORM EGG COLLECTOR?

PINWORM EGG COLLECTOR is a medical device that received FDA 510(k) clearance on 1995-04-05. The listed applicant is Evergreen Industries, Inc.. The 510(k) number is K950096.

When did PINWORM EGG COLLECTOR receive FDA 510(k) clearance?

PINWORM EGG COLLECTOR received FDA 510(k) clearance on 1995-04-05, under 510(k) number K950096.

Who is the listed applicant for PINWORM EGG COLLECTOR?

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

What is the FDA product code for PINWORM EGG COLLECTOR?

The FDA product code for PINWORM EGG COLLECTOR is LIO.

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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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