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FDA 510(k)

EXPRESSO CARTRIDGE

K-Number: K923316 · 1993-02-23

ApplicantBio-Rad Laboratories, Inc.
Decision Date1993-02-23
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

EXPRESSO CARTRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad Laboratories, Inc.. It received FDA 510(k) clearance on 1993-02-23 under 510(k) number K923316. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXPRESSO CARTRIDGE?

EXPRESSO CARTRIDGE is a medical device that received FDA 510(k) clearance on 1993-02-23. The listed applicant is Bio-Rad Laboratories, Inc.. The 510(k) number is K923316.

When did EXPRESSO CARTRIDGE receive FDA 510(k) clearance?

EXPRESSO CARTRIDGE received FDA 510(k) clearance on 1993-02-23, under 510(k) number K923316.

Who is the listed applicant for EXPRESSO CARTRIDGE?

The FDA 510(k) record lists Bio-Rad Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EXPRESSO CARTRIDGE?

The FDA product code for EXPRESSO CARTRIDGE is JQP.

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Related Devices (Code: JQP)

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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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