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)

COLUMBIA AGAR BASE

K-Number: K811641 · 1981-07-02

ApplicantHardy Media
Decision Date1981-07-02
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

COLUMBIA AGAR BASE is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1981-07-02 under 510(k) number K811641. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLUMBIA AGAR BASE?

COLUMBIA AGAR BASE is a medical device that received FDA 510(k) clearance on 1981-07-02. The listed applicant is Hardy Media. The 510(k) number is K811641.

When did COLUMBIA AGAR BASE receive FDA 510(k) clearance?

COLUMBIA AGAR BASE received FDA 510(k) clearance on 1981-07-02, under 510(k) number K811641.

Who is the listed applicant for COLUMBIA AGAR BASE?

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

What is the FDA product code for COLUMBIA AGAR BASE?

The FDA product code for COLUMBIA AGAR BASE is JSG.

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 Hardy Media 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 114 devices →

Related Devices (Code: JSG)

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.

↑