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)

MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM

K-Number: K862425 · 1986-07-02

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1986-07-02
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1986-07-02 under 510(k) number K862425. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM?

MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM is a medical device that received FDA 510(k) clearance on 1986-07-02. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K862425.

When did MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM receive FDA 510(k) clearance?

MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM received FDA 510(k) clearance on 1986-07-02, under 510(k) number K862425.

Who is the listed applicant for MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM?

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

What is the FDA product code for MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM?

The FDA product code for MACCONKEY AGAR W/MUG, DRI-FORM AND PRE-FORM is JSI.

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 Gibco Laboratories Life Technologies, 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.

K871855SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORMK871541MARTIN-LEWIS AGAR W/REDUCED VANCOMYCIN C0226K870134MCBRIDE LISTERIA AGAR W/CYCLOHEXIMIDE, DRI & PREK864755PSEUDOMONAS CEPACIA SELECTIVE AGAR, DRI & PRE-FORMK864014LOMBARD DOWELL AGAR BASEK863821MUELLER HINTON AGAR W/4%NACL AND OXACILLIN

View all 67 devices →

Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia Manufacturers, 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.

↑