CEFOPERAZONE 75MCG SENSIT- DISCS
K-Number: K821262 · 1982-06-22
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Device Summary
Frequently Asked Questions
What is the CEFOPERAZONE 75MCG SENSIT- DISCS?
CEFOPERAZONE 75MCG SENSIT- DISCS is a medical device that received FDA 510(k) clearance on 1982-06-22. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K821262.
When did CEFOPERAZONE 75MCG SENSIT- DISCS receive FDA 510(k) clearance?
CEFOPERAZONE 75MCG SENSIT- DISCS received FDA 510(k) clearance on 1982-06-22, under 510(k) number K821262.
Who is the listed applicant for CEFOPERAZONE 75MCG SENSIT- DISCS?
The FDA 510(k) record lists Difco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CEFOPERAZONE 75MCG SENSIT- DISCS?
The FDA product code for CEFOPERAZONE 75MCG SENSIT- DISCS 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 Difco Laboratories, Inc. 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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