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FDA 510(k)

PROP. CONQUEST C&B VLC GLAZE/SEALANT

K-Number: K953381 · 1995-09-27

ApplicantJeneric/Pentron, Inc.
Decision Date1995-09-27
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PROP. CONQUEST C&B VLC GLAZE/SEALANT 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 1995-09-27 under 510(k) number K953381. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROP. CONQUEST C&B VLC GLAZE/SEALANT?

PROP. CONQUEST C&B VLC GLAZE/SEALANT is a medical device that received FDA 510(k) clearance on 1995-09-27. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K953381.

When did PROP. CONQUEST C&B VLC GLAZE/SEALANT receive FDA 510(k) clearance?

PROP. CONQUEST C&B VLC GLAZE/SEALANT received FDA 510(k) clearance on 1995-09-27, under 510(k) number K953381.

Who is the listed applicant for PROP. CONQUEST C&B VLC GLAZE/SEALANT?

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 PROP. CONQUEST C&B VLC GLAZE/SEALANT?

The FDA product code for PROP. CONQUEST C&B VLC GLAZE/SEALANT is EBI.

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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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