CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK
K-Number: K821229 · 1982-06-22
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Device Summary
Frequently Asked Questions
What is the CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK?
CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is General Diagnostics. The 510(k) number is K821229.
When did CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK receive FDA 510(k) clearance?
CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821229.
Who is the listed applicant for CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK?
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 CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK?
The FDA product code for CEFOPERAZONE 75MCG. ANTIMICROBIAL DISK 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.
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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