FDA 510(k)

V AGAR

K-Number: K850844 · 1985-03-20

Decision Date1985-03-20

Product CodeJSH

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

V AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Micro Media Laboratories. It received FDA 510(k) clearance on 1985-03-20 under 510(k) number K850844. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V AGAR?

V AGAR is a medical device that received FDA 510(k) clearance on 1985-03-20. The listed applicant is Micro Media Laboratories. The 510(k) number is K850844.

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

V AGAR received FDA 510(k) clearance on 1985-03-20, under 510(k) number K850844.

Who is the listed applicant for V AGAR?

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

What is the FDA product code for V AGAR?

The FDA product code for V AGAR is JSH.

Other records listing Micro Media Laboratories 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.

K853690COLUMBIZ BLOOD AGAR K853691TERGITOL 7 AGAR K851344OXIDATIVE FORMENTIVE MEDIUM K851345PURPLE BROTH K851343BROM CRESOL PURPLE STARCH K851348COBA AGAR

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Related Devices (Code: JSH)

K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia 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.