RAPID FERMENTATION AGAR (RFA)
K-Number: K800734 · 1980-05-08
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Device Summary
Frequently Asked Questions
What is the RAPID FERMENTATION AGAR (RFA)?
RAPID FERMENTATION AGAR (RFA) is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is Remel Co.. The 510(k) number is K800734.
When did RAPID FERMENTATION AGAR (RFA) receive FDA 510(k) clearance?
RAPID FERMENTATION AGAR (RFA) received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800734.
Who is the listed applicant for RAPID FERMENTATION AGAR (RFA)?
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 RAPID FERMENTATION AGAR (RFA)?
The FDA product code for RAPID FERMENTATION AGAR (RFA) is JSE.
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: JSE)
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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