LKV AGAR, LKV ANAEROBIC AGAR
K-Number: K850554 · 1985-03-11
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Device Summary
Frequently Asked Questions
What is the LKV AGAR, LKV ANAEROBIC AGAR?
LKV AGAR, LKV ANAEROBIC AGAR is a medical device that received FDA 510(k) clearance on 1985-03-11. The listed applicant is Hardy Media. The 510(k) number is K850554.
When did LKV AGAR, LKV ANAEROBIC AGAR receive FDA 510(k) clearance?
LKV AGAR, LKV ANAEROBIC AGAR received FDA 510(k) clearance on 1985-03-11, under 510(k) number K850554.
Who is the listed applicant for LKV AGAR, LKV ANAEROBIC AGAR?
The FDA 510(k) record lists Hardy Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LKV AGAR, LKV ANAEROBIC AGAR?
The FDA product code for LKV AGAR, LKV ANAEROBIC AGAR is JSJ.
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 Hardy Media 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: JSJ)
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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