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FDA 510(k)

CONQUEST CRYSTAL

K-Number: K932154 · 1993-09-15

ApplicantJeneric/Pentron, Inc.
Decision Date1993-09-15
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CONQUEST CRYSTAL 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 1993-09-15 under 510(k) number K932154. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONQUEST CRYSTAL?

CONQUEST CRYSTAL is a medical device that received FDA 510(k) clearance on 1993-09-15. The listed applicant is Jeneric/Pentron, Inc.. The 510(k) number is K932154.

When did CONQUEST CRYSTAL receive FDA 510(k) clearance?

CONQUEST CRYSTAL received FDA 510(k) clearance on 1993-09-15, under 510(k) number K932154.

Who is the listed applicant for CONQUEST CRYSTAL?

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 CONQUEST CRYSTAL?

The FDA product code for CONQUEST CRYSTAL is EBF.

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Other records listing Jeneric/Pentron, Inc. as applicant

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Related Devices (Code: EBF)

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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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