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FDA 510(k)

MINI SAMPLE PROCESSOR

K-Number: K962859 · 1996-10-29

Decision Date1996-10-29
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINI SAMPLE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Cavro Scientific Instruments, Inc.. It received FDA 510(k) clearance on 1996-10-29 under 510(k) number K962859. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI SAMPLE PROCESSOR?

MINI SAMPLE PROCESSOR is a medical device that received FDA 510(k) clearance on 1996-10-29. The listed applicant is Cavro Scientific Instruments, Inc.. The 510(k) number is K962859.

When did MINI SAMPLE PROCESSOR receive FDA 510(k) clearance?

MINI SAMPLE PROCESSOR received FDA 510(k) clearance on 1996-10-29, under 510(k) number K962859.

Who is the listed applicant for MINI SAMPLE PROCESSOR?

The FDA 510(k) record lists Cavro Scientific Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI SAMPLE PROCESSOR?

The FDA product code for MINI SAMPLE PROCESSOR is JQW.

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 Cavro Scientific Instruments, 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.

Related Devices (Code: JQW)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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