PREPARED MACCONKEY AGAR
K-Number: K833508 · 1983-11-07
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Device Summary
Frequently Asked Questions
What is the PREPARED MACCONKEY AGAR?
PREPARED MACCONKEY AGAR is a medical device that received FDA 510(k) clearance on 1983-11-07. The listed applicant is Lavco Laboratory, Inc.. The 510(k) number is K833508.
When did PREPARED MACCONKEY AGAR receive FDA 510(k) clearance?
PREPARED MACCONKEY AGAR received FDA 510(k) clearance on 1983-11-07, under 510(k) number K833508.
Who is the listed applicant for PREPARED MACCONKEY AGAR?
The FDA 510(k) record lists Lavco Laboratory, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PREPARED MACCONKEY AGAR?
The FDA product code for PREPARED MACCONKEY 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 Lavco Laboratory, 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.
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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