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FDA 510(k)

CORRECT AND CORRECT FIT II

K-Number: K925331 · 1993-05-27

ApplicantJeneric/Pentron, Inc.
Decision Date1993-05-27
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CORRECT AND CORRECT FIT II is the device name listed in this FDA 510(k) record. The listed applicant is Jeneric/Pentron, Inc.. It received FDA 510(k) clearance on 1993-05-27 under 510(k) number K925331. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRECT AND CORRECT FIT II?

CORRECT AND CORRECT FIT II is a medical device that received FDA 510(k) clearance on 1993-05-27. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K925331.

When did CORRECT AND CORRECT FIT II receive FDA 510(k) clearance?

CORRECT AND CORRECT FIT II received FDA 510(k) clearance on 1993-05-27, under 510(k) number K925331.

Who is the listed applicant for CORRECT AND CORRECT FIT II?

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

What is the FDA product code for CORRECT AND CORRECT FIT II?

The FDA product code for CORRECT AND CORRECT FIT II is EJS.

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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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