MACCONKEY AGAR W/TWEEN 80 & AMPICIL
K-Number: K840190 · 1984-02-17
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Device Summary
Frequently Asked Questions
What is the MACCONKEY AGAR W/TWEEN 80 & AMPICIL?
MACCONKEY AGAR W/TWEEN 80 & AMPICIL is a medical device that received FDA 510(k) clearance on 1984-02-17. The listed applicant is Remel Co.. The 510(k) number is K840190.
When did MACCONKEY AGAR W/TWEEN 80 & AMPICIL receive FDA 510(k) clearance?
MACCONKEY AGAR W/TWEEN 80 & AMPICIL received FDA 510(k) clearance on 1984-02-17, under 510(k) number K840190.
Who is the listed applicant for MACCONKEY AGAR W/TWEEN 80 & AMPICIL?
The FDA 510(k) record lists Remel Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MACCONKEY AGAR W/TWEEN 80 & AMPICIL?
The FDA product code for MACCONKEY AGAR W/TWEEN 80 & AMPICIL 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 Remel Co. 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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