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)

CHOCOLATE AGAR & THAYER MARTIN AGAR

K-Number: K832612 · 1983-09-12

ApplicantCarroll Biological Corp.
Decision Date1983-09-12
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CHOCOLATE AGAR & THAYER MARTIN AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Carroll Biological Corp.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832612. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHOCOLATE AGAR & THAYER MARTIN AGAR?

CHOCOLATE AGAR & THAYER MARTIN AGAR is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Carroll Biological Corp.. The 510(k) number is K832612.

When did CHOCOLATE AGAR & THAYER MARTIN AGAR receive FDA 510(k) clearance?

CHOCOLATE AGAR & THAYER MARTIN AGAR received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832612.

Who is the listed applicant for CHOCOLATE AGAR & THAYER MARTIN AGAR?

The FDA 510(k) record lists Carroll Biological Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CHOCOLATE AGAR & THAYER MARTIN AGAR?

The FDA product code for CHOCOLATE AGAR & THAYER MARTIN AGAR is JTY.

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 Carroll Biological Corp. 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.

K832243CULTURE MEDIUM FOR ANTIMICROBIAL SUSK832617XYLOSE LYSINE DEOXYCHOLATEK832620TRYPTIC SOY BROTH MEDIAK832613MANNITOL SALT AGARK832615SF BROTHK832611TRYPTIC SOY AGAR

View all 11 devices →

Related Devices (Code: JTY)

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.

K210511InTray GCBiomed Diagnostics IncorporatedK993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, 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.

↑