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)

FRANKLIN COLLECTOR(R)

K-Number: K884612 · 1989-03-27

Decision Date1989-03-27
Product CodeFQZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

FRANKLIN COLLECTOR(R) is the device name listed in this FDA 510(k) record. The listed applicant is Franklin Diagnostics, Inc.. It received FDA 510(k) clearance on 1989-03-27 under 510(k) number K884612. The device is classified under product code FQZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRANKLIN COLLECTOR(R)?

FRANKLIN COLLECTOR(R) is a medical device that received FDA 510(k) clearance on 1989-03-27. The listed applicant is Franklin Diagnostics, Inc.. The 510(k) number is K884612.

When did FRANKLIN COLLECTOR(R) receive FDA 510(k) clearance?

FRANKLIN COLLECTOR(R) received FDA 510(k) clearance on 1989-03-27, under 510(k) number K884612.

Who is the listed applicant for FRANKLIN COLLECTOR(R)?

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

What is the FDA product code for FRANKLIN COLLECTOR(R)?

The FDA product code for FRANKLIN COLLECTOR(R) is FQZ.

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 Franklin Diagnostics, 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: FQZ)

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.

↑