FDA 510(k)

CIN AGAR

K-Number: K834327 · 1984-01-13

Decision Date1984-01-13

Product CodeJSF

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

CIN AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Hardy Media. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K834327. The device is classified under product code JSF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIN AGAR?

CIN AGAR is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Hardy Media. The 510(k) number is K834327.

When did CIN AGAR receive FDA 510(k) clearance?

CIN AGAR received FDA 510(k) clearance on 1984-01-13, under 510(k) number K834327.

Who is the listed applicant for CIN AGAR?

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 CIN AGAR?

The FDA product code for CIN AGAR is JSF.

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.

K880134MIDDLEBROOK 7H11 AGAR K880122MIDDLEBROOK 7H9 BROTH K880131LOWENSTEIN-JENSEN, GRUFT K880133MIL MEDIUM K880126LAURYL TRYPTOSE BROTH K880116MRVP BROTH

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Related Devices (Code: JSF)

K880946NUTRIENT GELATIN - PRODUCT NUMBER T2860Lakewood Biochemical Co., Inc.K880126LAURYL TRYPTOSE BROTHHardy Media K880119MOELLERS DECARBOXYLASE, ONITHINEHardy Media K880120MOELLERS DECARBOXYLASE, LYSINEHardy Media K880139ONPG TEST REAGENTHardy Media K880113CYSTINE TRYPTIC MEDIUM W/LACTOSEHardy Media

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.