CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP
K-Number: K831179 · 1983-05-09
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Device Summary
Frequently Asked Questions
What is the CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP?
CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP is a medical device that received FDA 510(k) clearance on 1983-05-09. The listed applicant is General Diagnostics. The 510(k) number is K831179.
When did CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP receive FDA 510(k) clearance?
CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP received FDA 510(k) clearance on 1983-05-09, under 510(k) number K831179.
Who is the listed applicant for CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP?
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 CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP?
The FDA product code for CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP 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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