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FDA 510(k)

JELENKO PORCELAIN SYSTEM PVS PROCELAIN

K-Number: K923717 · 1993-03-16

ApplicantJ.F. Jelenko & Co., Inc.
Decision Date1993-03-16
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JELENKO PORCELAIN SYSTEM PVS PROCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is J.F. Jelenko & Co., Inc.. It received FDA 510(k) clearance on 1993-03-16 under 510(k) number K923717. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JELENKO PORCELAIN SYSTEM PVS PROCELAIN?

JELENKO PORCELAIN SYSTEM PVS PROCELAIN is a medical device that received FDA 510(k) clearance on 1993-03-16. The listed applicant is J.F. Jelenko & Co., Inc.. The 510(k) number is K923717.

When did JELENKO PORCELAIN SYSTEM PVS PROCELAIN receive FDA 510(k) clearance?

JELENKO PORCELAIN SYSTEM PVS PROCELAIN received FDA 510(k) clearance on 1993-03-16, under 510(k) number K923717.

Who is the listed applicant for JELENKO PORCELAIN SYSTEM PVS PROCELAIN?

The FDA 510(k) record lists J.F. Jelenko & Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JELENKO PORCELAIN SYSTEM PVS PROCELAIN?

The FDA product code for JELENKO PORCELAIN SYSTEM PVS PROCELAIN is EIH.

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Other records listing J.F. Jelenko & Co., Inc. as applicant

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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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