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FDA 510(k)

LACTABACILLUS AGAR W/O TWEEN80

K-Number: K833292 · 1983-11-14

ApplicantAcumedia Manufacturers, Inc.
Decision Date1983-11-14
Product Code
DecisionSubstantially Equivalent

Device Summary

LACTABACILLUS AGAR W/O TWEEN80 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 1983-11-14 under 510(k) number K833292. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTABACILLUS AGAR W/O TWEEN80?

LACTABACILLUS AGAR W/O TWEEN80 is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833292.

When did LACTABACILLUS AGAR W/O TWEEN80 receive FDA 510(k) clearance?

LACTABACILLUS AGAR W/O TWEEN80 received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833292.

Who is the listed applicant for LACTABACILLUS AGAR W/O TWEEN80?

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

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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.

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