Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DENLEY WELLPREP 2 SAMPLE PROCESSOR

K-Number: K922327 · 1992-08-12

Decision Date1992-08-12
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DENLEY WELLPREP 2 SAMPLE PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Denley Instruments, Inc.. It received FDA 510(k) clearance on 1992-08-12 under 510(k) number K922327. 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 DENLEY WELLPREP 2 SAMPLE PROCESSOR?

DENLEY WELLPREP 2 SAMPLE PROCESSOR is a medical device that received FDA 510(k) clearance on 1992-08-12. The listed applicant is Denley Instruments, Inc.. The 510(k) number is K922327.

When did DENLEY WELLPREP 2 SAMPLE PROCESSOR receive FDA 510(k) clearance?

DENLEY WELLPREP 2 SAMPLE PROCESSOR received FDA 510(k) clearance on 1992-08-12, under 510(k) number K922327.

Who is the listed applicant for DENLEY WELLPREP 2 SAMPLE PROCESSOR?

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

What is the FDA product code for DENLEY WELLPREP 2 SAMPLE PROCESSOR?

The FDA product code for DENLEY WELLPREP 2 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 Denley 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.

View all 9 devices →

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

View on FDA Database →

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

↑