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FDA 510(k)

PIPERACILLIN 100MCG. ANTIMICROBIAL

K-Number: K820019 · 1982-01-29

Decision Date1982-01-29
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PIPERACILLIN 100MCG. ANTIMICROBIAL is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1982-01-29 under 510(k) number K820019. 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 PIPERACILLIN 100MCG. ANTIMICROBIAL?

PIPERACILLIN 100MCG. ANTIMICROBIAL is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is General Diagnostics. The 510(k) number is K820019.

When did PIPERACILLIN 100MCG. ANTIMICROBIAL receive FDA 510(k) clearance?

PIPERACILLIN 100MCG. ANTIMICROBIAL received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820019.

Who is the listed applicant for PIPERACILLIN 100MCG. ANTIMICROBIAL?

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 PIPERACILLIN 100MCG. ANTIMICROBIAL?

The FDA product code for PIPERACILLIN 100MCG. ANTIMICROBIAL 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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