FDA 510(k)

DEHYDRATED BILE

K-Number: K811358 · 1981-05-29

Decision Date1981-05-29

Product CodeJAK

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DEHYDRATED BILE 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 K811358. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEHYDRATED BILE?

DEHYDRATED BILE 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 K811358.

When did DEHYDRATED BILE receive FDA 510(k) clearance?

DEHYDRATED BILE received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811358.

Who is the listed applicant for DEHYDRATED BILE?

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 DEHYDRATED BILE?

The FDA product code for DEHYDRATED BILE is JAK.

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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.