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)

ZEFON GAS SAMPLING LINES

K-Number: K930957 · 1993-07-02

Decision Date1993-07-02
Product CodeCCK
Advisory CommitteeAN
DecisionUnknown

Device Summary

ZEFON GAS SAMPLING LINES is the device name listed in this FDA 510(k) record. The listed applicant is Zefon Medical Products. It received FDA 510(k) clearance on 1993-07-02 under 510(k) number K930957. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the ZEFON GAS SAMPLING LINES?

ZEFON GAS SAMPLING LINES is a medical device that received FDA 510(k) clearance on 1993-07-02. The listed applicant is Zefon Medical Products. The 510(k) number is K930957.

When did ZEFON GAS SAMPLING LINES receive FDA 510(k) clearance?

ZEFON GAS SAMPLING LINES received FDA 510(k) clearance on 1993-07-02, under 510(k) number K930957.

Who is the listed applicant for ZEFON GAS SAMPLING LINES?

The FDA 510(k) record lists Zefon Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEFON GAS SAMPLING LINES?

The FDA product code for ZEFON GAS SAMPLING LINES is CCK.

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 Zefon Medical Products 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: CCK)

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.

↑