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FDA 510(k)

PROCHEM EXT CHEMICAL INTEGRATOR

K-Number: K062651 · 2007-03-15

Decision Date2007-03-15
Product CodeJOJ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PROCHEM EXT CHEMICAL INTEGRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Raven Biological Laboratories, Inc.. It received FDA 510(k) clearance on 2007-03-15 under 510(k) number K062651. The device is classified under product code JOJ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCHEM EXT CHEMICAL INTEGRATOR?

PROCHEM EXT CHEMICAL INTEGRATOR is a medical device that received FDA 510(k) clearance on 2007-03-15. The listed applicant is Raven Biological Laboratories, Inc.. The 510(k) number is K062651.

When did PROCHEM EXT CHEMICAL INTEGRATOR receive FDA 510(k) clearance?

PROCHEM EXT CHEMICAL INTEGRATOR received FDA 510(k) clearance on 2007-03-15, under 510(k) number K062651.

Who is the listed applicant for PROCHEM EXT CHEMICAL INTEGRATOR?

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

What is the FDA product code for PROCHEM EXT CHEMICAL INTEGRATOR?

The FDA product code for PROCHEM EXT CHEMICAL INTEGRATOR is JOJ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Raven Biological Laboratories, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 15 devices →

Related Devices (Code: JOJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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