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FDA 510(k)

CORRECTED-V.P.S.

K-Number: K914178 · 1992-04-28

ApplicantJeneric/Pentron, Inc.
Decision Date1992-04-28
Product CodeELW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CORRECTED-V.P.S. 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 1992-04-28 under 510(k) number K914178. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRECTED-V.P.S.?

CORRECTED-V.P.S. is a medical device that received FDA 510(k) clearance on 1992-04-28. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K914178.

When did CORRECTED-V.P.S. receive FDA 510(k) clearance?

CORRECTED-V.P.S. received FDA 510(k) clearance on 1992-04-28, under 510(k) number K914178.

Who is the listed applicant for CORRECTED-V.P.S.?

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 CORRECTED-V.P.S.?

The FDA product code for CORRECTED-V.P.S. is ELW.

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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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