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FDA 510(k)

AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC

K-Number: K822809 · 1982-11-22

Decision Date1982-11-22
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1982-11-22 under 510(k) number K822809. 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 AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC?

AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC is a medical device that received FDA 510(k) clearance on 1982-11-22. The listed applicant is General Diagnostics. The 510(k) number is K822809.

When did AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC receive FDA 510(k) clearance?

AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC received FDA 510(k) clearance on 1982-11-22, under 510(k) number K822809.

Who is the listed applicant for AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC?

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 AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC?

The FDA product code for AZLOCILLIN 75 MCG SUSCEPTIBILITY DISC 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

View on FDA Database →

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

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