Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP

K-Number: K831179 · 1983-05-09

Decision Date1983-05-09
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CEFAZOLIN 30MCG. ANTIMICROBIAL SUSCEP is the device name listed in this FDA 510(k) record. The listed applicant is General Diagnostics. It received FDA 510(k) clearance on 1983-05-09 under 510(k) number K831179. 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 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.

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.

↑