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)

SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.

K-Number: K792349 · 1980-03-12

ApplicantPfizer, Inc.
Decision Date1980-03-12
Product CodeJNT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SUSCEPTIBILITY DISK, CINOXACIN 100 MCG. is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer, Inc.. It received FDA 510(k) clearance on 1980-03-12 under 510(k) number K792349. The device is classified under product code JNT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.?

SUSCEPTIBILITY DISK, CINOXACIN 100 MCG. is a medical device that received FDA 510(k) clearance on 1980-03-12. The listed applicant is Pfizer, Inc.. The 510(k) number is K792349.

When did SUSCEPTIBILITY DISK, CINOXACIN 100 MCG. receive FDA 510(k) clearance?

SUSCEPTIBILITY DISK, CINOXACIN 100 MCG. received FDA 510(k) clearance on 1980-03-12, under 510(k) number K792349.

Who is the listed applicant for SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.?

The FDA 510(k) record lists Pfizer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUSCEPTIBILITY DISK, CINOXACIN 100 MCG.?

The FDA product code for SUSCEPTIBILITY DISK, CINOXACIN 100 MCG. is JNT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Pfizer, 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.

K181102ThermaCare Quick Therapy TENSK991620VISINE FOR CONTACTSK892264ORALCHEK SUPER-SOFT BRUSHK892360WATER JEL STERILE GEL-SOAKED BURN DRESSINGK881378PFIZER HOSPITAL PRODUCTS GROUP ACL DRILL GUIDEK854726MEDI-WIPES UNITED ANTISEPTIC SKIN PREP

View all 30 devices →

Related Devices (Code: JNT)

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.

K922792ZITHROMAXDifco Laboratories, Inc.K914040PHOSPHOLIPID REAGENT SETSterling Diagnostics, Inc.

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.

↑