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FDA 510(k)

DEOXYCHOLATE LACTOSE AGAR

K-Number: K833203 · 1983-10-27

Decision Date1983-10-27
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DEOXYCHOLATE LACTOSE 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 1983-10-27 under 510(k) number K833203. 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 DEOXYCHOLATE LACTOSE AGAR?

DEOXYCHOLATE LACTOSE AGAR is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833203.

When did DEOXYCHOLATE LACTOSE AGAR receive FDA 510(k) clearance?

DEOXYCHOLATE LACTOSE AGAR received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833203.

Who is the listed applicant for DEOXYCHOLATE LACTOSE 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 DEOXYCHOLATE LACTOSE AGAR?

The FDA product code for DEOXYCHOLATE LACTOSE AGAR is JSI.

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 Acumedia Manufacturers, Inc. 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 177 devices →

Related Devices (Code: JSI)

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.

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