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FDA 510(k)

EZ VIEW

K-Number: K925693 · 1993-01-15

ApplicantDifco Laboratories, Inc.
Decision Date1993-01-15
Product CodeMDB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

EZ VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1993-01-15 under 510(k) number K925693. The device is classified under product code MDB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ VIEW?

EZ VIEW is a medical device that received FDA 510(k) clearance on 1993-01-15. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K925693.

When did EZ VIEW receive FDA 510(k) clearance?

EZ VIEW received FDA 510(k) clearance on 1993-01-15, under 510(k) number K925693.

Who is the listed applicant for EZ VIEW?

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

What is the FDA product code for EZ VIEW?

The FDA product code for EZ VIEW is MDB.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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