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FDA 510(k)

GENERAL DIAG. CEFONICID 30MCG ANTIMIC

K-Number: K842307 · 1984-07-20

Decision Date1984-07-20
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GENERAL DIAG. CEFONICID 30MCG ANTIMIC is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1984-07-20 under 510(k) number K842307. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GENERAL DIAG. CEFONICID 30MCG ANTIMIC?

GENERAL DIAG. CEFONICID 30MCG ANTIMIC is a medical device that received FDA 510(k) clearance on 1984-07-20. The listed applicant is General Diagnostics. The 510(k) number is K842307.

When did GENERAL DIAG. CEFONICID 30MCG ANTIMIC receive FDA 510(k) clearance?

GENERAL DIAG. CEFONICID 30MCG ANTIMIC received FDA 510(k) clearance on 1984-07-20, under 510(k) number K842307.

Who is the listed applicant for GENERAL DIAG. CEFONICID 30MCG ANTIMIC?

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

What is the FDA product code for GENERAL DIAG. CEFONICID 30MCG ANTIMIC?

The FDA product code for GENERAL DIAG. CEFONICID 30MCG ANTIMIC is JTN.

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 General Diagnostics 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 39 devices →

Related Devices (Code: JTN)

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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