FDA 510(k)

VIOLET RED BILE AGAR

K-Number: K811338 · 1981-05-29

Decision Date1981-05-29

Product CodeJSI

Advisory CommitteeMI

DecisionSubstantially Equivalent

Device Summary

VIOLET RED BILE AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Acumedia Manufacturers, Inc.. It received FDA 510(k) clearance on 1981-05-29 under 510(k) number K811338. 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 VIOLET RED BILE AGAR?

VIOLET RED BILE AGAR is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811338.

When did VIOLET RED BILE AGAR receive FDA 510(k) clearance?

VIOLET RED BILE AGAR received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811338.

Who is the listed applicant for VIOLET RED BILE AGAR?

The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VIOLET RED BILE AGAR?

The FDA product code for VIOLET RED BILE AGAR is JSI.

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Other records listing Acumedia Manufacturers, Inc. as applicant

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Related Devices (Code: JSI)

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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.